12-118474199-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118474199
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118474199
    reference: chr 12
allele count: 5
allele frequency: 4.119226903494752e-5
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.777C>T
  hgvsp: ENST00000315436.3:c.777C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*214C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.828C>T
  hgvsp: ENST00000441406.2:c.828C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.147C>T
  hgvsp: ENST00000544233.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.768C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.783C>T
  hgvsp: ENST00000535496.1:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.147C>T
  hgvsp: ENST00000543186.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.102C>T
  hgvsp: ENST00000542304.1:c.102C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.818C>T
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3473
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6747
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6806
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5775
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6310
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4609
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5441
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Tyr259Tyr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

12-118474199-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118474199
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118474199
    reference: chr 12
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.828C>A
  hgvsp: ENSP00000409131.2:p.Tyr276Ter
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.783C>A
  hgvsp: ENSP00000439450.1:p.Tyr261Ter
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.102C>A
  hgvsp: ENSP00000445941.1:p.Tyr34Ter
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.768C>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.147C>A
  hgvsp: ENSP00000445547.1:p.Tyr49Ter
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.147C>A
  hgvsp: ENSP00000444431.1:p.Tyr49Ter
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.777C>A
  hgvsp: ENSP00000319474.3:p.Tyr259Ter
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*214C>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.818C>A
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6747
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3473
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6806
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5441
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5775
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4609
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6310
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3593
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2105
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Tyr259Ter
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ

12-118474208-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118474208
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118474208
    reference: chr 12
allele count: 2
allele frequency: 1.647527884409444e-5
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.138G>A
  hgvsp: ENST00000543186.1:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.819G>A
  hgvsp: ENST00000441406.2:c.819G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.93G>A
  hgvsp: ENST00000542304.1:c.93G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*205G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.768G>A
  hgvsp: ENST00000315436.3:c.768G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.774G>A
  hgvsp: ENST00000535496.1:c.774G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.809G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.138G>A
  hgvsp: ENST00000544233.1:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.759G>A
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3475
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5449
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6751
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5780
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6805
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6750
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr256Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS

12-118474228-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118474228
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118474228
    reference: chr 12
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.73G>A
  hgvsp: ENSP00000445941.1:p.Asp25Asn
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.118G>A
  hgvsp: ENSP00000444431.1:p.Asp40Asn
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.739G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.754G>A
  hgvsp: ENSP00000439450.1:p.Asp252Asn
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.118G>A
  hgvsp: ENSP00000445547.1:p.Asp40Asn
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.799G>A
  hgvsp: ENSP00000409131.2:p.Asp267Asn
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*185G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.789G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.748G>A
  hgvsp: ENSP00000319474.3:p.Asp250Asn
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6749
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5449
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3476
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6798
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6751
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4520
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp250Asn
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

12-118474229-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118474229
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118474229
    reference: chr 12
allele count: 60
allele frequency: 4.94323518265254e-4
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.747C>T
  hgvsp: ENST00000315436.3:c.747C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.117C>T
  hgvsp: ENST00000543186.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.798C>T
  hgvsp: ENST00000441406.2:c.798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.738C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.117C>T
  hgvsp: ENST00000544233.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.753C>T
  hgvsp: ENST00000535496.1:c.753C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.72C>T
  hgvsp: ENST00000542304.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.788C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*184C>T
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 9.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6749
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6752
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3477
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6799
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3573
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro249Pro
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

12-118474232-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118474232
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118474232
    reference: chr 12
allele count: 3
allele frequency: 2.471739775236463e-5
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.114C>T
  hgvsp: ENST00000544233.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.750C>T
  hgvsp: ENST00000535496.1:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.114C>T
  hgvsp: ENST00000543186.1:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.795C>T
  hgvsp: ENST00000441406.2:c.795C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*181C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.69C>T
  hgvsp: ENST00000542304.1:c.69C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.785C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.744C>T
  hgvsp: ENST00000315436.3:c.744C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.735C>T
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6813
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6489
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5779
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6761
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6761
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3613
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser248Ser
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

12-118474238-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118474238
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118474238
    reference: chr 12
allele count: 517
allele frequency: 4.259982531599677e-3
allele num: 121362
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.738C>T
  hgvsp: ENST00000315436.3:c.738C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.789C>T
  hgvsp: ENST00000441406.2:c.789C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.63C>T
  hgvsp: ENST00000542304.1:c.63C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.729C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.108C>T
  hgvsp: ENST00000544233.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.779C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.744C>T
  hgvsp: ENST00000535496.1:c.744C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*175C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.108C>T
  hgvsp: ENST00000543186.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6803
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5739
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6759
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2373
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6289
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 6754
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6482
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 8.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 8.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 9.75e1
  variant carriers: 404
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 9.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5454
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 7.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp246Asp
num of homozygotes: 14
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ

12-118474240-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118474240
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118474240
    reference: chr 12
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.106G>A
  hgvsp: ENSP00000445547.1:p.Asp36Asn
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.787G>A
  hgvsp: ENSP00000409131.2:p.Asp263Asn
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*173G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.777G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.61G>A
  hgvsp: ENSP00000445941.1:p.Asp21Asn
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.727G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.106G>A
  hgvsp: ENSP00000444431.1:p.Asp36Asn
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.736G>A
  hgvsp: ENSP00000319474.3:p.Asp246Asn
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.742G>A
  hgvsp: ENSP00000439450.1:p.Asp248Asn
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5488
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6806
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4636
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3635
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asp246Asn
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: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

12-118474259-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118474259
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118474259
    reference: chr 12
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.87A>G
  hgvsp: ENST00000543186.1:c.87A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*154A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.42A>G
  hgvsp: ENST00000542304.1:c.42A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.723A>G
  hgvsp: ENST00000537945.1:c.723A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.723A>G
  hgvsp: ENST00000535496.1:c.723A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.717A>G
  hgvsp: ENST00000315436.3:c.717A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.87A>G
  hgvsp: ENST00000544233.1:c.87A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.768A>G
  hgvsp: ENST00000441406.2:c.768A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.708A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.758A>G
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5668
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4635
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6806
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6802
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6874
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3636
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gln239Gln
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

12-118474261-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118474261
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118474261
    reference: chr 12
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.85C>G
  hgvsp: ENSP00000444431.1:p.Gln29Glu
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.40C>G
  hgvsp: ENSP00000445941.1:p.Gln14Glu
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.766C>G
  hgvsp: ENSP00000409131.2:p.Gln256Glu
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.706C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.721C>G
  hgvsp: ENSP00000440386.1:p.Gln241Glu
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.756C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.85C>G
  hgvsp: ENSP00000445547.1:p.Gln29Glu
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.721C>G
  hgvsp: ENSP00000439450.1:p.Gln241Glu
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.715C>G
  hgvsp: ENSP00000319474.3:p.Gln239Glu
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*152C>G
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6806
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6802
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5488
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4635
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6521
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gln239Glu
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

12-118474273-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118474273
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118474273
    reference: chr 12
allele count: 1
allele frequency: 8.263506701703935e-6
allele num: 121014
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.709C>A
  hgvsp: ENSP00000440386.1:p.Leu237Ile
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.73C>A
  hgvsp: ENSP00000445547.1:p.Leu25Ile
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.744C>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*140C>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.754C>A
  hgvsp: ENSP00000409131.2:p.Leu252Ile
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.73C>A
  hgvsp: ENSP00000444431.1:p.Leu25Ile
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.28C>A
  hgvsp: ENSP00000445941.1:p.Leu10Ile
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.703C>A
  hgvsp: ENSP00000319474.3:p.Leu235Ile
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.709C>A
  hgvsp: ENSP00000439450.1:p.Leu237Ile
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.694C>A
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6803
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5488
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6804
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4635
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu235Ile
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

12-118474276-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118474276
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118474276
    reference: chr 12
allele count: 1
allele frequency: 8.269383434771103e-6
allele num: 120928
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.741A>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*137A>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.70A>C
  hgvsp: ENSP00000445547.1:p.Lys24Gln
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.751A>C
  hgvsp: ENSP00000409131.2:p.Lys251Gln
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.700A>C
  hgvsp: ENSP00000319474.3:p.Lys234Gln
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.70A>C
  hgvsp: ENSP00000444431.1:p.Lys24Gln
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.25A>C
  hgvsp: ENSP00000445941.1:p.Lys9Gln
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.706A>C
  hgvsp: ENSP00000440386.1:p.Lys236Gln
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.706A>C
  hgvsp: ENSP00000439450.1:p.Lys236Gln
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.691A>C
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5488
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4635
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6804
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3591
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Lys234Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS

12-118474278-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118474278
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118474278
    reference: chr 12
allele count: 1
allele frequency: 8.273899157717065e-6
allele num: 120862
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.704G>A
  hgvsp: ENSP00000439450.1:p.Arg235Gln
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.704G>A
  hgvsp: ENSP00000440386.1:p.Arg235Gln
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.689G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*135G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.749G>A
  hgvsp: ENSP00000409131.2:p.Arg250Gln
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.68G>A
  hgvsp: ENSP00000444431.1:p.Arg23Gln
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.739G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.68G>A
  hgvsp: ENSP00000445547.1:p.Arg23Gln
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.23G>A
  hgvsp: ENSP00000445941.1:p.Arg8Gln
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.698G>A
  hgvsp: ENSP00000319474.3:p.Arg233Gln
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6805
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4636
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6181
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg233Gln
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD

12-118474286-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118474286
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118474286
    reference: chr 12
allele count: 5
allele frequency: 4.148826711805902e-5
allele num: 120516
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.60G>A
  hgvsp: ENST00000543186.1:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.696G>A
  hgvsp: ENST00000535496.1:c.696G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*127G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.741G>A
  hgvsp: ENST00000441406.2:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.15G>A
  hgvsp: ENST00000542304.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.696G>A
  hgvsp: ENST00000537945.1:c.696G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.681G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.731G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.60G>A
  hgvsp: ENST00000544233.1:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.690G>A
  hgvsp: ENST00000315436.3:c.690G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5488
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6848
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4637
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6804
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr230Thr
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD

12-118474287-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118474287
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118474287
    reference: chr 12
allele count: 9
allele frequency: 7.467144563918757e-5
allele num: 120528
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.59C>T
  hgvsp: ENSP00000444431.1:p.Thr20Met
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.695C>T
  hgvsp: ENSP00000440386.1:p.Thr232Met
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.689C>T
  hgvsp: ENSP00000319474.3:p.Thr230Met
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.680C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.59C>T
  hgvsp: ENSP00000445547.1:p.Thr20Met
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.730C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.695C>T
  hgvsp: ENSP00000439450.1:p.Thr232Met
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.14C>T
  hgvsp: ENSP00000445941.1:p.Thr5Met
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*126C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.740C>T
  hgvsp: ENSP00000409131.2:p.Thr247Met
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6804
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6795
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6811
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6088
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr230Met
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

12-118474289-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118474289
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118474289
    reference: chr 12
allele count: 1
allele frequency: 8.304682179812978e-6
allele num: 120414
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.693C>T
  hgvsp: ENST00000535496.1:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.738C>T
  hgvsp: ENST00000441406.2:c.738C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.57C>T
  hgvsp: ENST00000543186.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.12C>T
  hgvsp: ENST00000542304.1:c.12C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.687C>T
  hgvsp: ENST00000315436.3:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.693C>T
  hgvsp: ENST00000537945.1:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.57C>T
  hgvsp: ENST00000544233.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*124C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.678C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.728C>T
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5005
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4638
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6793
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6806
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6036
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6804
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Tyr229Tyr
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

12-118474328-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118474328
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118474328
    reference: chr 12
allele count: 1
allele frequency: 8.490982576503753e-6
allele num: 117772
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.661-13T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.702-13T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-13T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.31-13T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.667-13T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.712-13T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-13T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.31-13T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.667-13T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*98-13T>C
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6785
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4971
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6801
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4637
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7832
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

12-118474332-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118474332
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118474332
    reference: chr 12
allele count: 7
allele frequency: 5.957953868414333e-5
allele num: 117490
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.702-17C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*98-17C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-17C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.661-17C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.31-17C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.667-17C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-17C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.31-17C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.712-17C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.667-17C>T
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6800
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5488
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6681
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4637
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2947
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4860
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6783
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6522
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7511
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ

12-118474334-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118474334
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118474334
    reference: chr 12
allele count: 1
allele frequency: 8.526312199447495e-6
allele num: 117284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-19C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-19C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.667-19C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.702-19C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.31-19C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.667-19C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*98-19C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.661-19C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.31-19C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.712-19C>T
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4636
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6669
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6799
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5488
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6782
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2033
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

12-118474345-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118474345
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118474345
    reference: chr 12
allele count: 2
allele frequency: 1.720430107526882e-5
allele num: 116250
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.702-30C>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.712-30C>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-30C>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.667-30C>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.31-30C>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.661-30C>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*98-30C>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-30C>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.31-30C>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.667-30C>A
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5487
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6792
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6759
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4636
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6548
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4557
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD

12-118474358-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118474358
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118474358
    reference: chr 12
allele count: 1
allele frequency: 8.708222303498963e-6
allele num: 114834
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.661-43C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.667-43C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.667-43C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.31-43C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-43C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.712-43C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.31-43C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.702-43C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-43C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*98-43C>G
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5487
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2655
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4632
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2388
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3461
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 838
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP

12-118474358-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118474358
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118474358
    reference: chr 12
allele count: 1
allele frequency: 8.708222303498963e-6
allele num: 114834
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*98-43C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.667-43C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.667-43C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.712-43C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.31-43C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-43C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.31-43C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.661-43C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.702-43C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-43C>T
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6516
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2655
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4632
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2388
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5487
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 838
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3461
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

12-118476042-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476042
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476042
    reference: chr 12
allele count: 2
allele frequency: 2.090650610469978e-5
allele num: 95664
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1727G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.701+51G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.666+51G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.30+51G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.666+51G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.30+51G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.711+51G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*97+51G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1727G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.660+51G>A
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21162
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14936
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8912
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3993
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

12-118476050-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476050
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476050
    reference: chr 12
allele count: 2
allele frequency: 2.081035523276382e-5
allele num: 96106
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.30+43G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1735G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.660+43G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*97+43G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.701+43G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.30+43G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.666+43G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.711+43G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.666+43G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1735G>C
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11091
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10508
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20904
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7980
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1738
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8758
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

12-118476052-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476052
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476052
    reference: chr 12
allele count: 2
allele frequency: 2.068894176062894e-5
allele num: 96670
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.666+41G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1737G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.30+41G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.711+41G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*97+41G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1737G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.30+41G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.660+41G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.666+41G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.701+41G>C
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11099
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9972
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20567
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1163
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1965
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP

12-118476054-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476054
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476054
    reference: chr 12
allele count: 1
allele frequency: 1.028446839582862e-5
allele num: 97234
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.666+39T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1739T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.30+39T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1739T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.711+39T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.30+39T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.660+39T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*97+39T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.666+39T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.701+39T>C
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8859
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11053
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10802
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum

12-118476055-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476055
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476055
    reference: chr 12
allele count: 2
allele frequency: 2.05672446062401e-5
allele num: 97242
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1740A>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.30+38A>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.660+38A>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.701+38A>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.30+38A>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.711+38A>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1740A>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.666+38A>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*97+38A>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.666+38A>C
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11055
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19857
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10909
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

12-118476064-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476064
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476064
    reference: chr 12
allele count: 1
allele frequency: 1.007617588972633e-5
allele num: 99244
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.666+29C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1749C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*97+29C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.660+29C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.701+29C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1749C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.30+29C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.30+29C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.711+29C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.666+29C>T
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4345
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10387
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14893
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6712
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1414
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

12-118476079-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476079
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476079
    reference: chr 12
allele count: 19809
allele frequency: 1.786042737354612e-1
allele num: 110910
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.666+14G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.711+14G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.30+14G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.666+14G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1764G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1764G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*97+14G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.30+14G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.660+14G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.701+14G>A
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.75e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 4.75e1
  variant carriers: 611
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 3.25e1
  variant carriers: 2932
genotype depth: GenotypeDepth
  all individuals: 27929
  bin: 2.25e1
  variant carriers: 3537
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 4.25e1
  variant carriers: 1046
genotype depth: GenotypeDepth
  all individuals: 9039
  bin: 2.75e1
  variant carriers: 3739
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.25e1
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.75e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.25e1
  variant carriers: 147
genotype depth: GenotypeDepth
  all individuals: 3546
  bin: 1.75e1
  variant carriers: 2380
genotype depth: GenotypeDepth
  all individuals: 4679
  bin: 7.5e0
  variant carriers: 146
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 3.75e1
  variant carriers: 1847
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 5.25e1
  variant carriers: 367
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.75e1
  variant carriers: 229
genotype depth: GenotypeDepth
  all individuals: 5072
  bin: 1.25e1
  variant carriers: 831
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 126
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 7.5e0
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 1561
  bin: 2.75e1
  variant carriers: 32
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 1.25e1
  variant carriers: 22
num of homozygotes: 1701
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

12-118476094-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476094
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476094
    reference: chr 12
allele count: 2
allele frequency: 1.693566142225685e-5
allele num: 118094
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.29C>T
  hgvsp: ENSP00000445547.1:p.Ser10Leu
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1779C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.29C>T
  hgvsp: ENSP00000444431.1:p.Ser10Leu
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1779C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.710C>T
  hgvsp: ENSP00000409131.2:p.Ser237Leu
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.665C>T
  hgvsp: ENSP00000439450.1:p.Ser222Leu
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.700C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.665C>T
  hgvsp: ENSP00000440386.1:p.Ser222Leu
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*96C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.659C>T
  hgvsp: ENSP00000319474.3:p.Ser220Leu
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3890
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14809
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser220Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/12-118476095-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476095
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476095
    reference: chr 12
allele count: 1
allele frequency: 8.450656616019065e-6
allele num: 118334
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.28T>G
  hgvsp: ENSP00000445547.1:p.Ser10Ala
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.699T>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.658T>G
  hgvsp: ENSP00000319474.3:p.Ser220Ala
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1780T>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.664T>G
  hgvsp: ENSP00000440386.1:p.Ser222Ala
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.28T>G
  hgvsp: ENSP00000444431.1:p.Ser10Ala
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.709T>G
  hgvsp: ENSP00000409131.2:p.Ser237Ala
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*95T>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1780T>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.664T>G
  hgvsp: ENSP00000439450.1:p.Ser222Ala
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser220Ala
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

12-118476096-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476096
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476096
    reference: chr 12
allele count: 1
allele frequency: 8.43540169382866e-6
allele num: 118548
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.663G>C
  hgvsp: ENSP00000439450.1:p.Lys221Asn
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.698G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.27G>C
  hgvsp: ENSP00000444431.1:p.Lys9Asn
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1781G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1781G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.663G>C
  hgvsp: ENSP00000440386.1:p.Lys221Asn
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.27G>C
  hgvsp: ENSP00000445547.1:p.Lys9Asn
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.708G>C
  hgvsp: ENSP00000409131.2:p.Lys236Asn
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.657G>C
  hgvsp: ENSP00000319474.3:p.Lys219Asn
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*94G>C
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14969
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36266
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Lys219Asn
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

12-118476103-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476103
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476103
    reference: chr 12
allele count: 1
allele frequency: 8.37184381488179e-6
allele num: 119448
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.701G>C
  hgvsp: ENSP00000409131.2:p.Gly234Ala
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.650G>C
  hgvsp: ENSP00000319474.3:p.Gly217Ala
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*87G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1788G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.656G>C
  hgvsp: ENSP00000439450.1:p.Gly219Ala
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.20G>C
  hgvsp: ENSP00000445547.1:p.Gly7Ala
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.656G>C
  hgvsp: ENSP00000440386.1:p.Gly219Ala
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.20G>C
  hgvsp: ENSP00000444431.1:p.Gly7Ala
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1788G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.691G>C
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15440
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36913
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1174
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly217Ala
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

12-118476109-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476109
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476109
    reference: chr 12
allele count: 1
allele frequency: 8.33541718763024e-6
allele num: 119970
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.695C>T
  hgvsp: ENSP00000409131.2:p.Ala232Val
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*81C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1794C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.14C>T
  hgvsp: ENSP00000444431.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1794C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.14C>T
  hgvsp: ENSP00000445547.1:p.Ala5Val
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.650C>T
  hgvsp: ENSP00000440386.1:p.Ala217Val
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.650C>T
  hgvsp: ENSP00000439450.1:p.Ala217Val
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.644C>T
  hgvsp: ENSP00000319474.3:p.Ala215Val
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.685C>T
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4985
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala215Val
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

12-118476125-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476125
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476125
    reference: chr 12
allele count: 1
allele frequency: 8.286239870071759e-6
allele num: 120682
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.634A>C
  hgvsp: ENSP00000439450.1:p.Ser212Arg
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.669A>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-3A>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-3A>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1810A>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.634A>C
  hgvsp: ENSP00000440386.1:p.Ser212Arg
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*65A>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.628A>C
  hgvsp: ENSP00000319474.3:p.Ser210Arg
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1810A>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.679A>C
  hgvsp: ENSP00000409131.2:p.Ser227Arg
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4037
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser210Arg
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

12-118476128-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476128
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476128
    reference: chr 12
allele count: 1
allele frequency: 8.283082632032337e-6
allele num: 120728
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.625T>A
  hgvsp: ENSP00000319474.3:p.Cys209Ser
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.676T>A
  hgvsp: ENSP00000409131.2:p.Cys226Ser
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-6T>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.666T>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.631T>A
  hgvsp: ENSP00000440386.1:p.Cys211Ser
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1813T>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.631T>A
  hgvsp: ENSP00000439450.1:p.Cys211Ser
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1813T>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-6T>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*62T>A
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Cys209Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

12-118476171-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476171
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476171
    reference: chr 12
allele count: 2
allele frequency: 1.656397005234214e-5
allele num: 120744
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.623G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*19G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.588G>C
  hgvsp: ENST00000537945.1:c.588G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.633G>C
  hgvsp: ENST00000441406.2:c.633G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.588G>C
  hgvsp: ENST00000535496.1:c.588G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-49G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-49G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.582G>C
  hgvsp: ENST00000315436.3:c.582G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1856G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1856G>C
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36582
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4994
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser194Ser
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP

12-118476171-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476171
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476171
    reference: chr 12
allele count: 1
allele frequency: 8.281985026171072e-6
allele num: 120744
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*19G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1856G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1856G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.582G>A
  hgvsp: ENST00000315436.3:c.582G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.633G>A
  hgvsp: ENST00000441406.2:c.633G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.588G>A
  hgvsp: ENST00000535496.1:c.588G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-49G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.588G>A
  hgvsp: ENST00000537945.1:c.588G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.623G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-49G>A
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36582
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser194Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

12-118476172-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476172
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476172
    reference: chr 12
allele count: 1
allele frequency: 8.285965232089886e-6
allele num: 120686
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.581C>T
  hgvsp: ENSP00000319474.3:p.Ser194Leu
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.587C>T
  hgvsp: ENSP00000439450.1:p.Ser196Leu
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1857C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*18C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-50C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.622C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.587C>T
  hgvsp: ENSP00000440386.1:p.Ser196Leu
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.632C>T
  hgvsp: ENSP00000409131.2:p.Ser211Leu
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1857C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-50C>T
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36452
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser194Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/12-118476178-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476178
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476178
    reference: chr 12
allele count: 1
allele frequency: 8.294487483618387e-6
allele num: 120562
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.626T>G
  hgvsp: ENSP00000409131.2:p.Val209Gly
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.575T>G
  hgvsp: ENSP00000319474.3:p.Val192Gly
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.616T>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-56T>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.581T>G
  hgvsp: ENSP00000440386.1:p.Val194Gly
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.581T>G
  hgvsp: ENSP00000439450.1:p.Val194Gly
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-56T>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.*12T>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1863T>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1863T>G
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16881
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1137
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Val192Gly
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

12-118476191-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476191
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476191
    reference: chr 12
allele count: 1
allele frequency: 8.345712807330875e-6
allele num: 119822
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.562A>G
  hgvsp: ENSP00000319474.3:p.Lys188Glu
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.603A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.613A>G
  hgvsp: ENSP00000409131.2:p.Lys205Glu
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1876A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.568A>G
  hgvsp: ENSP00000440386.1:p.Lys190Glu
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-69A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.568A>G
  hgvsp: ENSP00000439450.1:p.Lys190Glu
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1876A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.185A>G
  hgvsp: ENST00000543218.1:c.185A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-69A>G
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16675
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4028
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Lys188Glu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

12-118476201-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476201
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476201
    reference: chr 12
allele count: 5
allele frequency: 4.206771218954028e-5
allele num: 118856
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-71-8C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-8C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.611-8C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.566-8C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1886C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1886C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-8C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.601-8C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.566-8C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.560-8C>G
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32236
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3512
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45280
  bin: 6.25e1
  variant carriers: 0
hgvs: c.560-8C>G
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

12-118476219-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476219
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476219
    reference: chr 12
allele count: 1
allele frequency: 8.540730744922536e-6
allele num: 117086
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1904C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.601-26C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.611-26C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-71-26C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.566-26C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1904C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-26C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-26C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.560-26C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.566-26C>G
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12082
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6680
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23259
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2988
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3137
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7540
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

12-118476220-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476220
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476220
    reference: chr 12
allele count: 1
allele frequency: 8.546132020647455e-6
allele num: 117012
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-27T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.566-27T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.611-27T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1905T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-71-27T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-27T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.560-27T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.566-27T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.601-27T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1905T>C
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11615
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22633
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7305
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3573
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30548
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

12-118476228-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476228
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476228
    reference: chr 12
allele count: 9
allele frequency: 7.771886495915442e-5
allele num: 115802
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.566-35G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-71-35G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.566-35G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1913G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.560-35G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-35G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-35G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.611-35G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.601-35G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1913G>A
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16430
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14453
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13381
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9169
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8813
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1864
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD

12-118476233-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118476233
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118476233
    reference: chr 12
allele count: 6
allele frequency: 5.210504376823677e-5
allele num: 115152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.566-40G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.611-40G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.566-40G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-40G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-71-40G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-40G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.560-40G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.652-1918G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.601-40G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-15-1918G>A
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14790
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13485
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17233
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2572
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1044
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2546
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/12-118480597-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118480597
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118480597
    reference: chr 12
allele count: 1
allele frequency: 8.398280032249395e-6
allele num: 119072
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.565+49G>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536602
  gene symbol: WSB2
  hgvsc: ENST00000536602.1:n.672G>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-72+49G>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.559+49G>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.600+49G>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-4404G>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-16+49G>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.610+49G>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-4404G>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.565+49G>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.651+49G>T
  variant of: http://identifiers.org/hgnc/19222
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3850
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4531
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

12-118480604-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118480604
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118480604
    reference: chr 12
allele count: 1
allele frequency: 8.380965151946898e-6
allele num: 119318
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.559+42T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-72+42T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536602
  gene symbol: WSB2
  hgvsc: ENST00000536602.1:n.665T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.565+42T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.610+42T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.600+42T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-4411T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.565+42T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-4411T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.651+42T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-16+42T>C
  variant of: http://identifiers.org/hgnc/19222
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4531
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3850
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

12-118480609-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118480609
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118480609
    reference: chr 12
allele count: 2
allele frequency: 1.675687450776681e-5
allele num: 119354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536602
  gene symbol: WSB2
  hgvsc: ENST00000536602.1:n.660A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-72+37A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.565+37A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.600+37A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.610+37A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-4416A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-4416A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.651+37A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.565+37A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.559+37A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-16+37A>G
  variant of: http://identifiers.org/hgnc/19222
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4531
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3850
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

12-118480611-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118480611
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118480611
    reference: chr 12
allele count: 7
allele frequency: 5.861370220889923e-5
allele num: 119426
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-16+35A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.559+35A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-4418A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-4418A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.565+35A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.600+35A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.651+35A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536602
  gene symbol: WSB2
  hgvsc: ENST00000536602.1:n.658A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.565+35A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-72+35A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.610+35A>G
  variant of: http://identifiers.org/hgnc/19222
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4531
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3934
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3850
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4432
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

12-118480613-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118480613
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118480613
    reference: chr 12
allele count: 1
allele frequency: 8.374507997655138e-6
allele num: 119410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536602
  gene symbol: WSB2
  hgvsc: ENST00000536602.1:n.656C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.565+33C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.651+33C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.600+33C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-72+33C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-4420C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.610+33C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-16+33C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.565+33C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.559+33C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-4420C>T
  variant of: http://identifiers.org/hgnc/19222
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5592
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

12-118480618-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118480618
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118480618
    reference: chr 12
allele count: 1
allele frequency: 8.356592515835743e-6
allele num: 119666
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.651+28A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-4425A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.559+28A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536602
  gene symbol: WSB2
  hgvsc: ENST00000536602.1:n.651A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.565+28A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.610+28A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-4425A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.600+28A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.565+28A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-72+28A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-16+28A>G
  variant of: http://identifiers.org/hgnc/19222
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 875
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

12-118480621-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118480621
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118480621
    reference: chr 12
allele count: 1
allele frequency: 8.345155637152633e-6
allele num: 119830
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-4428G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-72+25G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-16+25G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.559+25G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536602
  gene symbol: WSB2
  hgvsc: ENST00000536602.1:n.648G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.651+25G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.565+25G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-4428G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.610+25G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.565+25G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.600+25G>A
  variant of: http://identifiers.org/hgnc/19222
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2753
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3851
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

12-118480622-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118480622
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118480622
    reference: chr 12
allele count: 2
allele frequency: 1.666083537428567e-5
allele num: 120042
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-72+24C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-16+24C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.600+24C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-4429C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.565+24C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.610+24C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-4429C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.559+24C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536602
  gene symbol: WSB2
  hgvsc: ENST00000536602.1:n.647C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.565+24C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.651+24C>T
  variant of: http://identifiers.org/hgnc/19222
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2869
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum

12-118480622-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118480622
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118480622
    reference: chr 12
allele count: 2
allele frequency: 1.666083537428567e-5
allele num: 120042
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-4429C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.610+24C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-4429C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.565+24C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-72+24C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536602
  gene symbol: WSB2
  hgvsc: ENST00000536602.1:n.647C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.651+24C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.565+24C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.600+24C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.559+24C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-16+24C>G
  variant of: http://identifiers.org/hgnc/19222
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2869
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5594
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5989
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

12-118480627-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118480627
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118480627
    reference: chr 12
allele count: 2
allele frequency: 1.662427476601333e-5
allele num: 120306
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-4434C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.600+19C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-72+19C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536602
  gene symbol: WSB2
  hgvsc: ENST00000536602.1:n.642C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.559+19C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-16+19C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.565+19C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.565+19C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.651+19C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-4434C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.610+19C>G
  variant of: http://identifiers.org/hgnc/19222
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4299
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3852
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2010
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS

12-118480630-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118480630
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118480630
    reference: chr 12
allele count: 1
allele frequency: 8.305647840531562e-6
allele num: 120400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.565+16G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.559+16G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-16+16G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.651+16G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-4437G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.565+16G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-4437G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.600+16G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.610+16G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536602
  gene symbol: WSB2
  hgvsc: ENST00000536602.1:n.639G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-72+16G>A
  variant of: http://identifiers.org/hgnc/19222
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

12-118480631-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118480631
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118480631
    reference: chr 12
allele count: 2
allele frequency: 1.660384877214538e-5
allele num: 120454
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.610+15G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.559+15G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.565+15G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.651+15G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-72+15G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-4438G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.600+15G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-4438G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-16+15G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536602
  gene symbol: WSB2
  hgvsc: ENST00000536602.1:n.638G>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.565+15G>C
  variant of: http://identifiers.org/hgnc/19222
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3924
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6420
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum

12-118480647-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118480647
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118480647
    reference: chr 12
allele count: 1
allele frequency: 8.256683785524381e-6
allele num: 121114
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.558C>T
  hgvsp: ENST00000315436.3:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-4454C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.564C>T
  hgvsp: ENST00000535496.1:c.564C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.599C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.564C>T
  hgvsp: ENST00000537945.1:c.564C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.650C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536602
  gene symbol: WSB2
  hgvsc: ENST00000536602.1:n.622C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-73C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-17C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.609C>T
  hgvsp: ENST00000441406.2:c.609C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-4454C>T
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.558C>T
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD

12-118480667-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118480667
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118480667
    reference: chr 12
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.544A>G
  hgvsp: ENSP00000439450.1:p.Ile182Val
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.579A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.589A>G
  hgvsp: ENSP00000409131.2:p.Ile197Val
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-4474A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.544A>G
  hgvsp: ENSP00000440386.1:p.Ile182Val
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-93A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.538A>G
  hgvsp: ENSP00000319474.3:p.Ile180Val
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536602
  gene symbol: WSB2
  hgvsc: ENST00000536602.1:n.602A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.630A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-4474A>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-37A>G
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4534
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3592
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile180Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: T
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

12-118480670-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118480670
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118480670
    reference: chr 12
allele count: 2
allele frequency: 1.648342591524222e-5
allele num: 121334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.627C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.576C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-96C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.541C>T
  hgvsp: ENSP00000440386.1:p.Arg181Cys
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.535C>T
  hgvsp: ENSP00000319474.3:p.Arg179Cys
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.541C>T
  hgvsp: ENSP00000439450.1:p.Arg181Cys
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.586C>T
  hgvsp: ENSP00000409131.2:p.Arg196Cys
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536602
  gene symbol: WSB2
  hgvsc: ENST00000536602.1:n.599C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-4477C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-40C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-4477C>T
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3920
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3613
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4534
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg179Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

12-118480671-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118480671
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118480671
    reference: chr 12
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.575T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-41T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-4478T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.540T>C
  hgvsp: ENST00000535496.1:c.540T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-4478T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536602
  gene symbol: WSB2
  hgvsc: ENST00000536602.1:n.598T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.534T>C
  hgvsp: ENST00000315436.3:c.534T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.540T>C
  hgvsp: ENST00000537945.1:c.540T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.585T>C
  hgvsp: ENST00000441406.2:c.585T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-97T>C
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.626T>C
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4631
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4534
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3918
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu178Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

12-118480673-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118480673
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118480673
    reference: chr 12
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-99C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.573C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.583C>G
  hgvsp: ENSP00000409131.2:p.Leu195Val
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.538C>G
  hgvsp: ENSP00000439450.1:p.Leu180Val
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.532C>G
  hgvsp: ENSP00000319474.3:p.Leu178Val
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-4480C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536602
  gene symbol: WSB2
  hgvsc: ENST00000536602.1:n.596C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.538C>G
  hgvsp: ENSP00000440386.1:p.Leu180Val
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-43C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-4480C>G
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.624C>G
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4634
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4534
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu178Val
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

12-118480683-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118480683
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118480683
    reference: chr 12
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-53G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445547
  ensembl transcript: ENST00000543186
  gene symbol: WSB2
  hgvsc: ENST00000543186.1:c.-109G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.614G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.528G>A
  hgvsp: ENST00000535496.1:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.573G>A
  hgvsp: ENST00000441406.2:c.573G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000542726
  gene symbol: WSB2
  hgvsc: ENST00000542726.1:n.587G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-4490G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.528G>A
  hgvsp: ENST00000537945.1:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536602
  gene symbol: WSB2
  hgvsc: ENST00000536602.1:n.586G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-4490G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.563G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.522G>A
  hgvsp: ENST00000315436.3:c.522G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4534
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg174Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

12-118480687-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118480687
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118480687
    reference: chr 12
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.524C>T
  hgvsp: ENSP00000439450.1:p.Ser175Leu
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.559C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.569C>T
  hgvsp: ENSP00000409131.2:p.Ser190Leu
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000542726
  gene symbol: WSB2
  hgvsc: ENST00000542726.1:n.583C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-4494C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.610C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536602
  gene symbol: WSB2
  hgvsc: ENST00000536602.1:n.582C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.518C>T
  hgvsp: ENSP00000319474.3:p.Ser173Leu
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-4494C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-57C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.524C>T
  hgvsp: ENSP00000440386.1:p.Ser175Leu
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4534
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser173Leu
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: G
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

12-118480689-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118480689
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118480689
    reference: chr 12
allele count: 2
allele frequency: 1.64766361299677e-5
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-59G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.608G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.522G>A
  hgvsp: ENST00000537945.1:c.522G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.557G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.522G>A
  hgvsp: ENST00000535496.1:c.522G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.567G>A
  hgvsp: ENST00000441406.2:c.567G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-4496G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000542726
  gene symbol: WSB2
  hgvsc: ENST00000542726.1:n.581G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.516G>A
  hgvsp: ENST00000315436.3:c.516G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536602
  gene symbol: WSB2
  hgvsc: ENST00000536602.1:n.580G>A
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-4496G>A
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5683
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4535
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala172Ala
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

12-118480690-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118480690
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118480690
    reference: chr 12
allele count: 3
allele frequency: 2.471413978317461e-5
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000542726
  gene symbol: WSB2
  hgvsc: ENST00000542726.1:n.580C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.556C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536602
  gene symbol: WSB2
  hgvsc: ENST00000536602.1:n.579C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-4497C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.566C>T
  hgvsp: ENSP00000409131.2:p.Ala189Val
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.521C>T
  hgvsp: ENSP00000439450.1:p.Ala174Val
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.521C>T
  hgvsp: ENSP00000440386.1:p.Ala174Val
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.607C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-4497C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-60C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.515C>T
  hgvsp: ENSP00000319474.3:p.Ala172Val
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5685
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2996
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala172Val
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

12-118480692-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118480692
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118480692
    reference: chr 12
allele count: 11
allele frequency: 9.061104795795647e-5
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.564C>T
  hgvsp: ENST00000441406.2:c.564C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.605C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-4499C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536602
  gene symbol: WSB2
  hgvsc: ENST00000536602.1:n.577C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.554C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.513C>T
  hgvsp: ENST00000315436.3:c.513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000542726
  gene symbol: WSB2
  hgvsc: ENST00000542726.1:n.578C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-62C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.519C>T
  hgvsp: ENST00000535496.1:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.519C>T
  hgvsp: ENST00000537945.1:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-4499C>T
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3916
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 4647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5686
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5597
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser171Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

12-118480718-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 118480718
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 118480718
    reference: chr 12
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000445941
  ensembl transcript: ENST00000542304
  gene symbol: WSB2
  hgvsc: ENST00000542304.1:c.-88C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000542726
  gene symbol: WSB2
  hgvsc: ENST00000542726.1:n.552C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000409131
  ensembl transcript: ENST00000441406
  gene symbol: WSB2
  hgvsc: ENST00000441406.2:c.538C>T
  hgvsp: ENSP00000409131.2:p.Pro180Ser
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000439450
  ensembl transcript: ENST00000535496
  gene symbol: WSB2
  hgvsc: ENST00000535496.1:c.493C>T
  hgvsp: ENSP00000439450.1:p.Pro165Ser
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000319474
  ensembl transcript: ENST00000315436
  gene symbol: WSB2
  hgvsc: ENST00000315436.3:c.487C>T
  hgvsp: ENSP00000319474.3:p.Pro163Ser
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000444431
  ensembl transcript: ENST00000544233
  gene symbol: WSB2
  hgvsc: ENST00000544233.1:c.-71-4525C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000438433
  ensembl transcript: ENST00000543218
  gene symbol: WSB2
  hgvsc: ENST00000543218.1:c.183-4525C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000540129
  gene symbol: WSB2
  hgvsc: ENST00000540129.1:n.528C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000176871
  ensembl protein: ENSP00000440386
  ensembl transcript: ENST00000537945
  gene symbol: WSB2
  hgvsc: ENST00000537945.1:c.493C>T
  hgvsp: ENSP00000440386.1:p.Pro165Ser
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536602
  gene symbol: WSB2
  hgvsc: ENST00000536602.1:n.551C>T
  variant of: http://identifiers.org/hgnc/19222
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000176871
  ensembl transcript: ENST00000536738
  gene symbol: WSB2
  hgvsc: ENST00000536738.1:n.579C>T
  variant of: http://identifiers.org/hgnc/19222
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3850
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro163Ser
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 4517
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3579
bin: 7.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2105
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3606
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3593
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29065
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1948
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12217
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.995024129972123e-5
allele num: 66722
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.932e1

FS
type: SiteQuality
SIO_000300: 5.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-1

QD
type: SiteQuality
SIO_000300: 1.286e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

DP
type: SiteQuality
SIO_000300: 2.804221e6

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

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

GenotypeQuality
all individuals: 1948
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3579
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29065
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12217
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3606
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4517
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.286e1

DP
type: SiteQuality
SIO_000300: 2.804221e6

VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.94e-1

FS
type: SiteQuality
SIO_000300: 5.33e-1

MQ
type: SiteQuality
SIO_000300: 5.932e1

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

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

GenotypeQuality
all individuals: 4523
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12235
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1949
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2107
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29055
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3611
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3596
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3583
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.46e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

VQSLOD
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

QD
type: SiteQuality
SIO_000300: 1.345e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.80134e6

MQRankSum
type: SiteQuality
SIO_000300: -6.899999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.757e0

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

GenotypeQuality
all individuals: 29055
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1948
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3609
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2106
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 12229
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3575
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3596
bin: 9.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.482e1

MQ
type: SiteQuality
SIO_000300: 5.954e1

FS
type: SiteQuality
SIO_000300: 2.736e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.88e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.360000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.800875e6

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12223
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3596
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 3609
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 27
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29060
bin: 9.75e1
variant carriers: 60

GenotypeQuality
all individuals: 1948
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2104
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4516
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.818181818181818e-4
allele num: 16500
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 49
allele frequency: 7.344344854462064e-4
allele num: 66718
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.318535152876144e-4
allele num: 11578
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.87e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.15e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

QD
type: SiteQuality
SIO_000300: 1.442e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.49e-1

DP
type: SiteQuality
SIO_000300: 2.801134e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.72e0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4525
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 0
bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997781641585227e-5
allele num: 66716
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
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SIO_000300: 4.59e0

BaseQRankSum
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SIO_000300: -1.043e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.558e1

DP
type: SiteQuality
SIO_000300: 2.795673e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.0e-3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 502

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

South Asian
type: Population
allele count: 1
allele frequency: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

Latino
type: Population
allele count: 31
allele frequency: 2.678417141869708e-3
allele num: 11574
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 4.405286343612335e-3
allele num: 908
num of homozygotes: 0

African
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allele count: 473
allele frequency: 4.546328335255671e-2
allele num: 10404
num of homozygotes: 14

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
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allele count: 8
allele frequency: 1.199184554502938e-4
allele num: 66712
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.887e0

MQRankSum
type: SiteQuality
SIO_000300: 2.79e-1

ReadPosRankSum
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SIO_000300: 6.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.98e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.23e-2

FS
type: SiteQuality
SIO_000300: 5.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.03e-1

DP
type: SiteQuality
SIO_000300: 2.807534e6

QD
type: SiteQuality
SIO_000300: 1.404e1

MQ
type: SiteQuality
SIO_000300: 5.977e1

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -5.791e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.761585e6

QD
type: SiteQuality
SIO_000300: 1.309e1

VQSLOD
type: SiteQuality
SIO_000300: -1.175e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.28e-1

FS
type: SiteQuality
SIO_000300: 6.394e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.214e0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.081245439065921e-5
allele num: 16444
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.759902e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

FS
type: SiteQuality
SIO_000300: 3.331e0

VQSLOD
type: SiteQuality
SIO_000300: -1.527e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.56e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.515e-1

QD
type: SiteQuality
SIO_000300: 3.342e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.285e0

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66662
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.954e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-1

QD
type: SiteQuality
SIO_000300: 1.386e1

FS
type: SiteQuality
SIO_000300: 2.331e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.41e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.759734e6

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16304
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501726986033939e-5
allele num: 66590
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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-2

FS
type: SiteQuality
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InbreedingCoeff
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QD
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MQ
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VQSLOD
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DP
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
type: SiteQuality
SIO_000300: -4.422e0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66572
num of homozygotes: 0

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

Latino
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allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16248
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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MQRankSum
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SIO_000300: 6.22e-1

InbreedingCoeff
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VQSLOD
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BaseQRankSum
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QD
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MQ
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DP
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ClippingRankSum
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SIO_000300: -4.32e-1

ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 6.921e0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502448991856726e-5
allele num: 66558
num of homozygotes: 0

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

Other
type: Population
allele count: 0
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allele num: 900
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East Asian
type: Population
allele count: 0
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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ClippingRankSum
type: SiteQuality
SIO_000300: 2.24e-1

VQSLOD
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.985e1

DP
type: SiteQuality
SIO_000300: 2.753682e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.72e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.0e-1

FS
type: SiteQuality
SIO_000300: 1.472e0

QD
type: SiteQuality
SIO_000300: 1.064e1

GenotypeQuality
all individuals: 11239
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
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GenotypeQuality
all individuals: 2099
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GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
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GenotypeQuality
all individuals: 63
bin: 4.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1958
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28822
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 74
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 5.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.877816725087632e-4
allele num: 15976
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157139551029854e-4
allele num: 8642
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.925e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.55e-1

DP
type: SiteQuality
SIO_000300: 2.748323e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

VQSLOD
type: SiteQuality
SIO_000300: 5.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.53e-1

FS
type: SiteQuality
SIO_000300: 2.574e0

QD
type: SiteQuality
SIO_000300: 1.152e1

GenotypeQuality
all individuals: 3576
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2097
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 29
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9

GenotypeQuality
all individuals: 115
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variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.253908692933083e-5
allele num: 15990
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 6.919218128351496e-4
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66456
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.968e1

DP
type: SiteQuality
SIO_000300: 2.747645e6

VQSLOD
type: SiteQuality
SIO_000300: 2.46e0

QD
type: SiteQuality
SIO_000300: 1.226e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.389e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.47e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e-1

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3622
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 118
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variant carriers: 0

GenotypeQuality
all individuals: 28815
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 1959
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GenotypeQuality
all individuals: 863
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 71
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variant carriers: 0

GenotypeQuality
all individuals: 79
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variant carriers: 0

GenotypeQuality
all individuals: 11236
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15914
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66420
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.97e-1

QD
type: SiteQuality
SIO_000300: 1.319e1

MQRankSum
type: SiteQuality
SIO_000300: 1.38e-1

DP
type: SiteQuality
SIO_000300: 2.745077e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.953e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.368e0

FS
type: SiteQuality
SIO_000300: 1.845e0

VQSLOD
type: SiteQuality
SIO_000300: 9.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.39e-1

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4137
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variant carriers: 0

GenotypeQuality
all individuals: 3418
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 166
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GenotypeQuality
all individuals: 1956
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variant carriers: 0

GenotypeQuality
all individuals: 225
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variant carriers: 0

GenotypeQuality
all individuals: 49
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variant carriers: 0

GenotypeQuality
all individuals: 2039
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variant carriers: 0

GenotypeQuality
all individuals: 56
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variant carriers: 0

GenotypeQuality
all individuals: 3605
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GenotypeQuality
all individuals: 28810
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 516
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variant carriers: 0

GenotypeQuality
all individuals: 3530
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variant carriers: 0

GenotypeQuality
all individuals: 3607
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14178
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.735202492211838e-5
allele num: 10272
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 2.695373e6

MQRankSum
type: SiteQuality
SIO_000300: 2.07e0

FS
type: SiteQuality
SIO_000300: 1.922e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.985e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.1e-1

QD
type: SiteQuality
SIO_000300: 1.881e1

VQSLOD
type: SiteQuality
SIO_000300: -2.352e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.59e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.31e0

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

GenotypeQuality
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GenotypeQuality
all individuals: 231
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variant carriers: 0

GenotypeQuality
all individuals: 24
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GenotypeQuality
all individuals: 70
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 600
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 7

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3607
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1955
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.067073170731707e-4
allele num: 65600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14008
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10252
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.690398e6

VQSLOD
type: SiteQuality
SIO_000300: 3.08e0

QD
type: SiteQuality
SIO_000300: 1.357e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.07e0

FS
type: SiteQuality
SIO_000300: 6.75e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3531
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GenotypeQuality
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GenotypeQuality
all individuals: 52
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7271
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variant carriers: 0

GenotypeQuality
all individuals: 4110
bin: 6.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13878
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.525692664469669e-5
allele num: 65544
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10238
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.76e-1

FS
type: SiteQuality
SIO_000300: 2.693e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.3e-2

DP
type: SiteQuality
SIO_000300: 2.686816e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.134e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 9.57e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3510
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.737317581653926e-4
allele num: 11512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65274
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13186
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.913e0

DP
type: SiteQuality
SIO_000300: 2.674624e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

QD
type: SiteQuality
SIO_000300: 1.594e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

MQRankSum
type: SiteQuality
SIO_000300: 3.57e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.081e0

VQSLOD
type: SiteQuality
SIO_000300: 4.94e-1

GenotypeQuality
all individuals: 726
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 930
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 511
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GenotypeQuality
all individuals: 1970
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3851
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 28788
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variant carriers: 1

GenotypeQuality
all individuals: 1939
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12220
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.540832049306625e-5
allele num: 64900
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10194
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.7e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.165e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: 3.92e-1

QD
type: SiteQuality
SIO_000300: 1.328e1

DP
type: SiteQuality
SIO_000300: 2.65485e6

GenotypeQuality
all individuals: 511
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2901
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.540832049306625e-5
allele num: 64900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12220
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10194
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.97e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.53e-1

DP
type: SiteQuality
SIO_000300: 2.65485e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.165e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.7e0

QD
type: SiteQuality
SIO_000300: 1.328e1

GenotypeQuality
all individuals: 298
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 718
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.689492325855962e-5
allele num: 54208
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4782
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11958
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8832
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6662
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.926e0

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.67e0

QD
type: SiteQuality
SIO_000300: 1.625e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.55e-1

DP
type: SiteQuality
SIO_000300: 9.23489e5

GenotypeQuality
all individuals: 788
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 268
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 803
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10369
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variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6692
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4830
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.674579260674653e-5
allele num: 54428
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 716
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12036
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.194e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.46e-1

QD
type: SiteQuality
SIO_000300: 1.028e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.32e-1

DP
type: SiteQuality
SIO_000300: 9.48763e5

GenotypeQuality
all individuals: 187
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8710
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 801
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GenotypeQuality
all individuals: 10687
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variant carriers: 0

GenotypeQuality
all individuals: 1361
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variant carriers: 0

GenotypeQuality
all individuals: 11434
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 549
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variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8920
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.385041551246537e-3
allele num: 722
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6738
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54710
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.229098090849243e-5
allele num: 12152
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 7.83e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.543e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.47e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.25e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.60271e5

GenotypeQuality
all individuals: 665
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3026
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 12878
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variant carriers: 0

GenotypeQuality
all individuals: 5054
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GenotypeQuality
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GenotypeQuality
all individuals: 684
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1164
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 818
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variant carriers: 0

GenotypeQuality
all individuals: 8608
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6804
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4892
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8968
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12258
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.160092807424594e-4
allele num: 8620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54970
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 722
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.84e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.72426e5

VQSLOD
type: SiteQuality
SIO_000300: -2.533e0

MQRankSum
type: SiteQuality
SIO_000300: 1.53e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.84e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.123e0

GenotypeQuality
all individuals: 5006
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8530
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
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GenotypeQuality
all individuals: 691
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GenotypeQuality
all individuals: 2867
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3123
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GenotypeQuality
all individuals: 1164
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 13785
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12258
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.324500232450023e-4
allele num: 8604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6804
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54984
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8968
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4894
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.02e0

DP
type: SiteQuality
SIO_000300: 9.79108e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -6.6e-1

QD
type: SiteQuality
SIO_000300: 1.453e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.99e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1173
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 1
allele frequency: 1.089561996077577e-4
allele num: 9178
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 752
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5020
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8730
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56048
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6992
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12524
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.06776e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.691e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.055e0

FS
type: SiteQuality
SIO_000300: 5.441e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.02e0

QD
type: SiteQuality
SIO_000300: 6.76e0

MQRankSum
type: SiteQuality
SIO_000300: 8.070000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.03e-1

GenotypeQuality
all individuals: 613
bin: 7.25e1
variant carriers: 100

GenotypeQuality
all individuals: 4842
bin: 2.25e1
variant carriers: 22

GenotypeQuality
all individuals: 1226
bin: 3.75e1
variant carriers: 66

GenotypeQuality
all individuals: 182
bin: 1.75e1
variant carriers: 18

GenotypeQuality
all individuals: 321
bin: 9.25e1
variant carriers: 138

GenotypeQuality
all individuals: 565
bin: 4.25e1
variant carriers: 51

GenotypeQuality
all individuals: 639
bin: 4.75e1
variant carriers: 127

GenotypeQuality
all individuals: 702
bin: 5.25e1
variant carriers: 129

GenotypeQuality
all individuals: 17387
bin: 9.75e1
variant carriers: 16741

GenotypeQuality
all individuals: 2049
bin: 3.25e1
variant carriers: 48

GenotypeQuality
all individuals: 190
bin: 2.5e0
variant carriers: 3

GenotypeQuality
all individuals: 213
bin: 8.75e1
variant carriers: 91

GenotypeQuality
all individuals: 496
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variant carriers: 79

GenotypeQuality
all individuals: 508
bin: 8.25e1
variant carriers: 153

GenotypeQuality
all individuals: 699
bin: 7.75e1
variant carriers: 169

GenotypeQuality
all individuals: 26049
bin: 6.25e1
variant carriers: 133

GenotypeQuality
all individuals: 2178
bin: 6.75e1
variant carriers: 167

European (Non-Finnish)
type: Population
allele count: 11196
allele frequency: 1.807905955302933e-1
allele num: 61928
num of homozygotes: 968

Latino
type: Population
allele count: 1967
allele frequency: 1.865162146785511e-1
allele num: 10546
num of homozygotes: 184

South Asian
type: Population
allele count: 2916
allele frequency: 2.03375645138792e-1
allele num: 14338
num of homozygotes: 299

Other
type: Population
allele count: 156
allele frequency: 1.921182266009852e-1
allele num: 812
num of homozygotes: 12

African
type: Population
allele count: 1754
allele frequency: 1.836264656616415e-1
allele num: 9552
num of homozygotes: 134

European (Finnish)
type: Population
allele count: 833
allele frequency: 1.469654199011997e-1
allele num: 5668
num of homozygotes: 48

East Asian
type: Population
allele count: 987
allele frequency: 1.223654847508059e-1
allele num: 8066
num of homozygotes: 56

VQSLOD
type: SiteQuality
SIO_000300: 6.49e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.56e-1

DP
type: SiteQuality
SIO_000300: 1.420839e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.06e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.491e0

QD
type: SiteQuality
SIO_000300: 1.65e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

African
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allele count: 2
allele frequency: 1.98294665873488e-4
allele num: 10086
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65370
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6216
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11334
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
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SIO_000300: 3.232e0

DP
type: SiteQuality
SIO_000300: 1.443338e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.89e-1

QD
type: SiteQuality
SIO_000300: 1.046e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.83e-1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 329
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10102
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65472
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6238
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.366993505666624e-5
allele num: 15706
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e0

DP
type: SiteQuality
SIO_000300: 1.445859e6

VQSLOD
type: SiteQuality
SIO_000300: 6.5e-1

FS
type: SiteQuality
SIO_000300: 1.647e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

QD
type: SiteQuality
SIO_000300: 1.563e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.827e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 152
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GenotypeQuality
all individuals: 1159
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11370
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.162790697674419e-4
allele num: 8600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65546
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6274
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15762
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.1e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.450282e6

QD
type: SiteQuality
SIO_000300: 1.301e1

MQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.25e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 271
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1145
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 222
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.79431929480901e-5
allele num: 10210
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65920
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6378
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15994
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.97e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.82e-1

QD
type: SiteQuality
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VQSLOD
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SIO_000300: -8.075e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.54e0

DP
type: SiteQuality
SIO_000300: 1.466685e6

GenotypeQuality
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variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66128
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6430
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10236
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.181998021760633e-5
allele num: 16176
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.41e-1

QD
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.954e1

VQSLOD
type: SiteQuality
SIO_000300: 7.5e-1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16376
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Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66402
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.888e0

InbreedingCoeff
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.488086e6

ClippingRankSum
type: SiteQuality
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505570611261668e-5
allele num: 66420
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.38e-1

FS
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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BaseQRankSum
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SIO_000300: 6.6e-2

InbreedingCoeff
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MQ
type: SiteQuality
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Latino
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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

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.010687942194791e-5
allele num: 66430
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.02e-1

VQSLOD
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FS
type: SiteQuality
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BaseQRankSum
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MQ
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MQRankSum
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SIO_000300: 2.38e-1

InbreedingCoeff
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SIO_000300: 1.0e-4

ClippingRankSum
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SIO_000300: -4.46e-1

QD
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 1.157407407407407e-4
allele num: 8640
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11528
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 frequency: 0.0e0
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66430
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10308
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South Asian
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e0

DP
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MQ
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VQSLOD
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FS
type: SiteQuality
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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QD
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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 1.157943492357573e-4
allele num: 8636
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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

Latino
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: 1.13e0

VQSLOD
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ClippingRankSum
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DP
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InbreedingCoeff
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MQ
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MQRankSum
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FS
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6554
num of homozygotes: 0

Other
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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 frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.506977304921788e-5
allele num: 66358
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.584e0

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6516
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
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African
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allele count: 1
allele frequency: 9.780907668231612e-5
allele num: 10224
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66022
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East Asian
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num of homozygotes: 0

QD
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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DP
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FS
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MQ
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.623810685533057e-5
allele num: 65584
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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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South Asian
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East Asian
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Other
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MQRankSum
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DP
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QD
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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FS
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MQ
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InbreedingCoeff
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Non-Finnish)
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num of homozygotes: 0

South Asian
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European (Finnish)
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Other
type: Population
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num of homozygotes: 0

Latino
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FS
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MQ
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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DP
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BaseQRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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European (Finnish)
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Other
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African
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East Asian
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European (Non-Finnish)
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allele num: 64686
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QD
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BaseQRankSum
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DP
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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FS
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 9

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 850
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.247699553947409e-4
allele num: 64118
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15146
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11110
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6344
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.197891710589363e-4
allele num: 8348
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9874
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.31e-1

FS
type: SiteQuality
SIO_000300: 1.058e0

DP
type: SiteQuality
SIO_000300: 1.208704e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.53e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.855e0

QD
type: SiteQuality
SIO_000300: 1.162e1

GenotypeQuality
all individuals: 93
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 749
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GenotypeQuality
all individuals: 2612
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9824
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.701162754254552e-5
allele num: 63814
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14986
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11030
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.607503607503608e-4
allele num: 8316
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6324
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.973e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.225e1

VQSLOD
type: SiteQuality
SIO_000300: 4.95e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.182953e6

GenotypeQuality
all individuals: 74
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1592
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44730
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514508996183437e-5
allele num: 66028
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14968
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.537e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

VQSLOD
type: SiteQuality
SIO_000300: -1.929e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.529e0

DP
type: SiteQuality
SIO_000300: 3.436884e6

QD
type: SiteQuality
SIO_000300: 1.43e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.35e-1

GenotypeQuality
all individuals: 161
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1699
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 847
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 44730
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 77
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variant carriers: 0

GenotypeQuality
all individuals: 1592
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66074
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15154
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.626492106276473e-5
allele num: 10388
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 9.21e-1

QD
type: SiteQuality
SIO_000300: 1.285e1

DP
type: SiteQuality
SIO_000300: 3.44032e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.88e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.883e0

MQ
type: SiteQuality
SIO_000300: 5.875e1

VQSLOD
type: SiteQuality
SIO_000300: -1.845e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.632e0

GenotypeQuality
all individuals: 1591
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1730
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variant carriers: 0

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

GenotypeQuality
all individuals: 297
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variant carriers: 0

GenotypeQuality
all individuals: 856
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variant carriers: 0

GenotypeQuality
all individuals: 44728
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 499
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GenotypeQuality
all individuals: 4208
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GenotypeQuality
all individuals: 39
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 45
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GenotypeQuality
all individuals: 721
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 924
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GenotypeQuality
all individuals: 331
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variant carriers: 0

GenotypeQuality
all individuals: 1365
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
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GenotypeQuality
all individuals: 1285
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GenotypeQuality
all individuals: 879
bin: 3.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.025810160670519e-5
allele num: 66098
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15164
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.94e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.189e0

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.319e-1

DP
type: SiteQuality
SIO_000300: 3.443681e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.73e-1

QD
type: SiteQuality
SIO_000300: 1.522e1

GenotypeQuality
all individuals: 862
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1591
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 925
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.058873358746294e-4
allele num: 66108
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15226
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.21e-2

MQ
type: SiteQuality
SIO_000300: 5.958e1

FS
type: SiteQuality
SIO_000300: 6.19e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.43e0

DP
type: SiteQuality
SIO_000300: 3.445705e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

QD
type: SiteQuality
SIO_000300: 1.517e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.26e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 924
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GenotypeQuality
all individuals: 862
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15222
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66102
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: -1.058e0

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -6.042e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.0e-1

DP
type: SiteQuality
SIO_000300: 3.447128e6

GenotypeQuality
all individuals: 444
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variant carriers: 0

GenotypeQuality
all individuals: 907
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511487303506651e-5
allele num: 66160
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15404
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.231e1

ClippingRankSum
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FS
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MQ
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SIO_000300: 5.934e1

DP
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SIO_000300: 3.453186e6

BaseQRankSum
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SIO_000300: 3.3e-1

InbreedingCoeff
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SIO_000300: 1.48e-2

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 7.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.67e-1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66198
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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allele num: 10396
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11570
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

South Asian
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allele frequency: 6.390593047034765e-5
allele num: 15648
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.508978421608571e-5
allele num: 66270
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

InbreedingCoeff
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SIO_000300: 9.8e-3

MQRankSum
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SIO_000300: 2.65e-1

VQSLOD
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BaseQRankSum
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SIO_000300: 2.74e0

QD
type: SiteQuality
SIO_000300: 1.242e1

FS
type: SiteQuality
SIO_000300: 5.96e-1

MQ
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SIO_000300: 5.956e1

DP
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SIO_000300: 3.464277e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.49e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15648
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508978421608571e-5
allele num: 66270
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.58e-1

MQRankSum
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SIO_000300: 2.65e-1

BaseQRankSum
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QD
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InbreedingCoeff
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SIO_000300: 9.8e-3

ClippingRankSum
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SIO_000300: -8.49e-1

FS
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SIO_000300: 5.96e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

ReadPosRankSum
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SIO_000300: 1.68e0

DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15836
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.922337562475971e-4
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66336
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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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

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

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

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

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

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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allele frequency: 1.922337562475971e-4
allele num: 10404
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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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66370
num of homozygotes: 0

South Asian
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East Asian
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allele frequency: 0.0e0
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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FS
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ClippingRankSum
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MQ
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VQSLOD
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South 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

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: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

East Asian
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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MQ
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DP
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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Latino
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African
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South Asian
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Other
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QD
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FS
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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MQ
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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Other
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European (Non-Finnish)
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South Asian
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VQSLOD
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FS
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QD
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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Latino
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African
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European (Non-Finnish)
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Other
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East Asian
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ClippingRankSum
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VQSLOD
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MQRankSum
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FS
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MQ
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ReadPosRankSum
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DP
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BaseQRankSum
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QD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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European (Non-Finnish)
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East Asian
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African
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Latino
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European (Finnish)
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InbreedingCoeff
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BaseQRankSum
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FS
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ClippingRankSum
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VQSLOD
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MQRankSum
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DP
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ReadPosRankSum
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MQ
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QD
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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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South Asian
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East Asian
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European (Finnish)
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African
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Latino
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Other
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InbreedingCoeff
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ClippingRankSum
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FS
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ReadPosRankSum
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VQSLOD
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DP
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MQ
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BaseQRankSum
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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European (Non-Finnish)
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East Asian
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European (Finnish)
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Latino
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Other
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MQ
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QD
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InbreedingCoeff
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BaseQRankSum
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DP
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FS
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VQSLOD
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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African
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European (Finnish)
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European (Non-Finnish)
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South Asian
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East Asian
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QD
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DP
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InbreedingCoeff
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MQRankSum
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VQSLOD
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BaseQRankSum
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MQ
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ClippingRankSum
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FS
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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African
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.66e-1

DP
type: SiteQuality
SIO_000300: 3.48881e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 4.08e-1

QD
type: SiteQuality
SIO_000300: 1.269e1

MQRankSum
type: SiteQuality
SIO_000300: 4.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.121e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.46e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

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

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2205
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1406
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7385
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1599
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44730
bin: 9.75e1
variant carriers: 11

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

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1408
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 931
bin: 8.75e1
variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 6.909656244601831e-4
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.489196e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.0e-3

MQ
type: SiteQuality
SIO_000300: 5.963e1

VQSLOD
type: SiteQuality
SIO_000300: 4.86e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 5.47e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.313e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.19e-1