5-113698898-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113698898
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113698898
    reference: chr 5
allele count: 1
allele frequency: 8.572212316554656e-6
allele num: 116656
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.95C>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.426C>G
  hgvsp: ENST00000264773.3:c.426C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.426C>G
  hgvsp: ENST00000512097.3:c.426C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Gly142Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

5-113698910-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113698910
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113698910
    reference: chr 5
allele count: 2
allele frequency: 1.734545202247971e-5
allele num: 115304
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.438C>T
  hgvsp: ENST00000512097.3:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.438C>T
  hgvsp: ENST00000264773.3:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.107C>T
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Ile146Ile
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ

5-113698911-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113698911
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113698911
    reference: chr 5
allele count: 1
allele frequency: 8.702008423544154e-6
allele num: 114916
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.439G>A
  hgvsp: ENSP00000427120.3:p.Val147Met
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.439G>A
  hgvsp: ENSP00000264773.2:p.Val147Met
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.108G>A
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 661
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Val147Met
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

5-113698923-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113698923
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113698923
    reference: chr 5
allele count: 1
allele frequency: 9.043553754883519e-6
allele num: 110576
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.451A>G
  hgvsp: ENSP00000427120.3:p.Ile151Val
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.120A>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.451A>G
  hgvsp: ENSP00000264773.2:p.Ile151Val
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Ile151Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/5-113698931-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113698931
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113698931
    reference: chr 5
allele count: 1
allele frequency: 9.387732111676462e-6
allele num: 106522
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.128C>A
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
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  hgvsp: ENST00000264773.3:c.459C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.459C>A
  hgvsp: ENST00000512097.3:c.459C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Thr153Thr
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
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site quality: QD
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5-113698931-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113698931
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113698931
    reference: chr 5
allele count: 1
allele frequency: 9.387732111676462e-6
allele num: 106522
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.459C>T
  hgvsp: ENST00000512097.3:c.459C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.459C>T
  hgvsp: ENST00000264773.3:c.459C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.128C>T
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Thr153Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
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site quality: InbreedingCoeff
site quality: QD
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5-113698952-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113698952
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113698952
    reference: chr 5
allele count: 1
allele frequency: 1.142230547813771e-5
allele num: 87548
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.480C>T
  hgvsp: ENST00000512097.3:c.480C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.149C>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.480C>T
  hgvsp: ENST00000264773.3:c.480C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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hgvs: p.Tyr160Tyr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: DP
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site quality: FS
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site quality: QD

5-113698954-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113698954
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113698954
    reference: chr 5
allele count: 2
allele frequency: 2.311604253351826e-5
allele num: 86520
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.482A>G
  hgvsp: ENSP00000264773.2:p.Asp161Gly
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.482A>G
  hgvsp: ENSP00000427120.3:p.Asp161Gly
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
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  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.151A>G
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Asp161Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
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5-113698962-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113698962
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113698962
    reference: chr 5
allele count: 1
allele frequency: 1.2966468711911e-5
allele num: 77122
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.486+4C>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.155+4C>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
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canonical: true
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: c.486+4C>T
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
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site quality: VQSLOD
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5-113698965-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
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    reference: chr 5
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    type: ExactPosition
    position: 113698965
    reference: chr 5
allele count: 1
allele frequency: 1.332232021528869e-5
allele num: 75062
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.155+7G>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.486+7G>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.486+7G>T
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: c.486+7G>T
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
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site quality: QD
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5-113698972-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113698972
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113698972
    reference: chr 5
allele count: 1
allele frequency: 1.526204938799182e-5
allele num: 65522
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.155+14C>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.486+14C>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
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  ensembl protein: ENSP00000427120
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  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.486+14C>T
  variant of: http://identifiers.org/hgnc/6291
canonical: true
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: BaseQRankSum
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site quality: QD
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site quality: MQ
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site quality: VQSLOD

http://identifiers.org/exac.variant/5-113698974-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113698974
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113698974
    reference: chr 5
allele count: 2
allele frequency: 3.14901121047991e-5
allele num: 63512
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.486+16C>A
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.486+16C>A
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.155+16C>A
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
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genotype depth: GenotypeDepth
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num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: QD
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5-113698974-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113698974
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113698974
    reference: chr 5
allele count: 4
allele frequency: 6.298022420959819e-5
allele num: 63512
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.486+16C>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.155+16C>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
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  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.486+16C>G
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
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5-113698979-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113698979
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113698979
    reference: chr 5
allele count: 5
allele frequency: 8.545255674049768e-5
allele num: 58512
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.486+21C>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.155+21C>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
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  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.486+21C>G
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
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5-113698982-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113698982
    reference: chr 5
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    type: ExactPosition
    position: 113698982
    reference: chr 5
allele count: 1
allele frequency: 1.812513593851954e-5
allele num: 55172
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.486+24C>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.155+24C>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
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  ensembl protein: ENSP00000427120
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  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.486+24C>T
  variant of: http://identifiers.org/hgnc/6291
canonical: true
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genotype depth: GenotypeDepth
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num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
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5-113698994-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113698994
    reference: chr 5
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    type: ExactPosition
    position: 113698993
    reference: chr 5
allele count: 5
allele frequency: 1.153136531365314e-4
allele num: 43360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.486+39delG
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.486+39delG
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.155+39delG
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
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genotype depth: GenotypeDepth
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num of homozygotes: 0
population: Other
population: African
population: Latino
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population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: CG
site quality: BaseQRankSum
site quality: ClippingRankSum
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5-113698995-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113698995
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113698995
    reference: chr 5
allele count: 1
allele frequency: 2.35626767200754e-5
allele num: 42440
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
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  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.486+37G>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.486+37G>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
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  consequence: non_coding_transcript_variant
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  ensembl gene: ENSG00000080709
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  gene symbol: KCNN2
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  variant of: http://identifiers.org/hgnc/6291
canonical: true
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

5-113699001-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699001
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699001
    reference: chr 5
allele count: 1
allele frequency: 2.670940170940171e-5
allele num: 37440
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.486+43T>C
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.155+43T>C
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.486+43T>C
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 8.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
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site quality: ClippingRankSum

5-113699553-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699553
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699553
    reference: chr 5
allele count: 1
allele frequency: 8.394050297149381e-6
allele num: 119132
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.156-50G>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.487-50G>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.487-50G>T
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

5-113699554-GTTAAAAGTGCTTCTTTC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699554
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699537
    reference: chr 5
allele count: 7
allele frequency: 5.872286164893795e-5
allele num: 119204
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: GTTAAAAGTGCTTCTTTC
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
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5-113699561-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699561
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699561
    reference: chr 5
allele count: 3
allele frequency: 2.512352399296541e-5
allele num: 119410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.487-42G>A
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.487-42G>A
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.156-42G>A
  variant of: http://identifiers.org/hgnc/6291
canonical: true
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filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
  all individuals: 161
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ

5-113699570-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699570
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699570
    reference: chr 5
allele count: 10
allele frequency: 8.35282325425994e-5
allele num: 119720
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.487-33T>C
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.156-33T>C
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.487-33T>C
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2399
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

5-113699578-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699578
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699578
    reference: chr 5
allele count: 1
allele frequency: 8.328197611472925e-6
allele num: 120074
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.156-25G>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.487-25G>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.487-25G>T
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5725
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

5-113699584-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699584
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699584
    reference: chr 5
allele count: 1
allele frequency: 8.307441806370146e-6
allele num: 120374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.487-19C>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.487-19C>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.156-19C>T
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

5-113699586-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699586
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699586
    reference: chr 5
allele count: 1
allele frequency: 8.297928836962294e-6
allele num: 120512
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.156-17G>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.487-17G>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.487-17G>T
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10448
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

5-113699587-TCTGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699587
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699583
    reference: chr 5
allele count: 2
allele frequency: 1.658952537367906e-5
allele num: 120558
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.487-12_487-9delACTG
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.156-12_156-9delACTG
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.487-12_487-9delACTG
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: TCTGA
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
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site quality: QD

5-113699588-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699588
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699588
    reference: chr 5
allele count: 2
allele frequency: 1.658539821541115e-5
allele num: 120588
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.487-15C>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.487-15C>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.156-15C>G
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
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site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
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site quality: MQ

5-113699594-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699594
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699594
    reference: chr 5
allele count: 1
allele frequency: 8.273899157717065e-6
allele num: 120862
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.156-9G>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.487-9G>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.487-9G>T
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5725
  bin: 4.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD

5-113699608-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699608
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699608
    reference: chr 5
allele count: 4
allele frequency: 3.302509907529722e-5
allele num: 121120
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.492G>C
  hgvsp: ENST00000512097.3:c.492G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.492G>C
  hgvsp: ENST00000264773.3:c.492G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.161G>C
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Ser164Ser
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

5-113699621-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699621
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699621
    reference: chr 5
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.505G>T
  hgvsp: ENSP00000264773.2:p.Ala169Ser
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.505G>T
  hgvsp: ENSP00000427120.3:p.Ala169Ser
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.174G>T
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Ala169Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD

5-113699651-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699651
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699651
    reference: chr 5
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.204A>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.535A>G
  hgvsp: ENSP00000427120.3:p.Ile179Val
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.535A>G
  hgvsp: ENSP00000264773.2:p.Ile179Val
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Ile179Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
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site quality: VQSLOD

5-113699653-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699653
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699653
    reference: chr 5
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.206C>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.537C>T
  hgvsp: ENST00000512097.3:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.537C>T
  hgvsp: ENST00000264773.3:c.537C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Ile179Ile
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
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site quality: DP

5-113699654-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699654
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699654
    reference: chr 5
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.207A>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.538A>G
  hgvsp: ENSP00000427120.3:p.Ile180Val
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.538A>G
  hgvsp: ENSP00000264773.2:p.Ile180Val
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 777
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Ile180Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
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site quality: QD
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site quality: DP
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site quality: InbreedingCoeff

5-113699656-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699656
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699656
    reference: chr 5
allele count: 10
allele frequency: 8.240626287597858e-5
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.540C>T
  hgvsp: ENST00000512097.3:c.540C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.540C>T
  hgvsp: ENST00000264773.3:c.540C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.209C>T
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Ile180Ile
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum

5-113699662-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699662
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699662
    reference: chr 5
allele count: 3
allele frequency: 2.472187886279357e-5
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.215C>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.546C>T
  hgvsp: ENST00000512097.3:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.546C>T
  hgvsp: ENST00000264773.3:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Leu182Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD

5-113699663-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699663
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699663
    reference: chr 5
allele count: 2
allele frequency: 1.648179585647652e-5
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.547G>T
  hgvsp: ENSP00000427120.3:p.Gly183Cys
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.547G>T
  hgvsp: ENSP00000264773.2:p.Gly183Cys
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.216G>T
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Gly183Cys
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: ReadPosRankSum
site quality: MQRankSum
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site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
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5-113699666-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699666
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699666
    reference: chr 5
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.550C>G
  hgvsp: ENSP00000264773.2:p.Leu184Val
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.550C>G
  hgvsp: ENSP00000427120.3:p.Leu184Val
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.219C>G
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 325
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Leu184Val
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
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site quality: QD
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5-113699671-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699671
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699671
    reference: chr 5
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.555C>T
  hgvsp: ENST00000512097.3:c.555C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.224C>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.555C>T
  hgvsp: ENST00000264773.3:c.555C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 21221
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ile185Ile
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

5-113699672-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699672
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699672
    reference: chr 5
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.225A>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.556A>G
  hgvsp: ENSP00000427120.3:p.Ile186Val
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.556A>G
  hgvsp: ENSP00000264773.2:p.Ile186Val
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 1027
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 21221
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  variant carriers: 1
hgvs: p.Ile186Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP

5-113699676-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699676
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699676
    reference: chr 5
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.560T>C
  hgvsp: ENSP00000427120.3:p.Val187Ala
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.229T>C
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.560T>C
  hgvsp: ENSP00000264773.2:p.Val187Ala
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2401
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Val187Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

5-113699683-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699683
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699683
    reference: chr 5
allele count: 53
allele frequency: 4.368755976128458e-4
allele num: 121316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.567C>T
  hgvsp: ENST00000264773.3:c.567C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.567C>T
  hgvsp: ENST00000512097.3:c.567C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.236C>T
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.His189His
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/5-113699687-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699687
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699687
    reference: chr 5
allele count: 23
allele frequency: 1.896281639046912e-4
allele num: 121290
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.571A>C
  hgvsp: ENST00000512097.3:c.571A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.240A>C
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.571A>C
  hgvsp: ENST00000264773.3:c.571A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 23
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg191Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum

5-113699692-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699692
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699692
    reference: chr 5
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.245A>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.576A>G
  hgvsp: ENST00000264773.3:c.576A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.576A>G
  hgvsp: ENST00000512097.3:c.576A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3657
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  variant carriers: 0
hgvs: p.Glu192Glu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

5-113699704-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699704
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699704
    reference: chr 5
allele count: 1
allele frequency: 8.250144377526608e-6
allele num: 121210
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+6T>C
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.582+6T>C
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.582+6T>C
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.25e1
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 1
hgvs: c.582+6T>C
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

5-113699704-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699704
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699704
    reference: chr 5
allele count: 1
allele frequency: 8.250144377526608e-6
allele num: 121210
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.582+6T>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.582+6T>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+6T>G
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: c.582+6T>G
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
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site quality: ClippingRankSum

5-113699707-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699707
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699707
    reference: chr 5
allele count: 2
allele frequency: 1.650600818698006e-5
allele num: 121168
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+9G>A
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.582+9G>A
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.582+9G>A
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.75e1
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genotype quality: GenotypeQuality
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  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 3005
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

5-113699710-CCTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699710
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699707
    reference: chr 5
allele count: 1
allele frequency: 8.255865792645674e-6
allele num: 121126
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.582+16_582+18delCTG
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.582+16_582+18delCTG
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+16_251+18delCTG
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1464
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 3.25e1
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genotype depth: GenotypeDepth
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  bin: 3.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3655
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: CCTG
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

5-113699724-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699724
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699724
    reference: chr 5
allele count: 2
allele frequency: 1.652510162937502e-5
allele num: 121028
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+26A>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.582+26A>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.582+26A>G
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 3.75e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

5-113699726-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699726
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699726
    reference: chr 5
allele count: 1
allele frequency: 8.263233568560049e-6
allele num: 121018
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.582+28G>A
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+28G>A
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.582+28G>A
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

http://identifiers.org/exac.variant/5-113699727-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699727
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699727
    reference: chr 5
allele count: 1
allele frequency: 8.264736024331383e-6
allele num: 120996
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+29A>C
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.582+29A>C
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.582+29A>C
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

5-113699736-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699736
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699736
    reference: chr 5
allele count: 10
allele frequency: 8.271161767381847e-5
allele num: 120902
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.582+38C>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+38C>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.582+38C>G
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3774
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 6.25e1
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genotype depth: GenotypeDepth
  all individuals: 25
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genotype depth: GenotypeDepth
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  variant carriers: 2
genotype depth: GenotypeDepth
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  bin: 1.25e1
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genotype depth: GenotypeDepth
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  bin: 5.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 2
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 780
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 7.25e1
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genotype depth: GenotypeDepth
  all individuals: 475
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genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 5337
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum

5-113699738-TAC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699738
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699736
    reference: chr 5
allele count: 3
allele frequency: 2.481759070829404e-5
allele num: 120882
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+42_251+43delCA
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.582+42_582+43delCA
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.582+42_582+43delCA
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 3774
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genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 9.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2305
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: TAC
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

5-113699739-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699739
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699739
    reference: chr 5
allele count: 1
allele frequency: 8.273214640280627e-6
allele num: 120872
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.582+41A>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+41A>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.582+41A>G
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8135
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
reference allele: A
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

5-113699741-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699741
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699741
    reference: chr 5
allele count: 1
allele frequency: 8.275953389830508e-6
allele num: 120832
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+43A>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.582+43A>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.582+43A>G
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

5-113699744-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113699744
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113699744
    reference: chr 5
allele count: 1
allele frequency: 8.283906027370025e-6
allele num: 120716
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+46C>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.582+46C>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
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  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.582+46C>T
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
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site quality: MQ
site quality: VQSLOD

5-113740088-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113740088
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113740088
    reference: chr 5
allele count: 5
allele frequency: 4.415556890034971e-5
allele num: 113236
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.583-47G>A
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+40390G>A
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.583-47G>A
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
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site quality: DP
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5-113740096-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113740096
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113740096
    reference: chr 5
allele count: 2
allele frequency: 1.76230086000282e-5
allele num: 113488
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.583-39A>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.583-39A>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+40398A>G
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
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site quality: VQSLOD

5-113740098-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113740098
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113740098
    reference: chr 5
allele count: 1
allele frequency: 8.810262193402876e-6
allele num: 113504
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.583-37G>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.583-37G>T
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+40400G>T
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1717
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genotype depth: GenotypeDepth
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num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
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site quality: FS
site quality: QD

http://identifiers.org/exac.variant/5-113740107-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113740107
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113740107
    reference: chr 5
allele count: 1
allele frequency: 8.768545473676827e-6
allele num: 114044
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.583-28A>C
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+40409A>C
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.583-28A>C
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 348
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ

5-113740112-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113740112
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113740112
    reference: chr 5
allele count: 1
allele frequency: 8.732861758798358e-6
allele num: 114510
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.583-23G>A
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+40414G>A
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.583-23G>A
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
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site quality: InbreedingCoeff
site quality: MQ
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site quality: DP
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site quality: QD

5-113740112-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113740112
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113740112
    reference: chr 5
allele count: 4
allele frequency: 3.493144703519343e-5
allele num: 114510
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+40414G>C
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.583-23G>C
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.583-23G>C
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
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site quality: MQRankSum

5-113740120-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113740120
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113740120
    reference: chr 5
allele count: 2
allele frequency: 1.729505361466621e-5
allele num: 115640
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+40422A>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.583-15A>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.583-15A>G
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
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site quality: VQSLOD

5-113740141-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113740141
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113740141
    reference: chr 5
allele count: 1
allele frequency: 8.345573507811457e-6
allele num: 119824
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.589A>G
  hgvsp: ENSP00000427120.3:p.Met197Val
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+40443A>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.589A>G
  hgvsp: ENSP00000264773.2:p.Met197Val
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 340
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Met197Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

5-113740144-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113740144
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113740144
    reference: chr 5
allele count: 1
allele frequency: 8.321959988016378e-6
allele num: 120164
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.592G>A
  hgvsp: ENSP00000264773.2:p.Val198Met
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.592G>A
  hgvsp: ENSP00000427120.3:p.Val198Met
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+40446G>A
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3584
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  variant carriers: 0
hgvs: p.Val198Met
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

5-113740151-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113740151
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113740151
    reference: chr 5
allele count: 2
allele frequency: 1.657715005636231e-5
allele num: 120648
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.599A>G
  hgvsp: ENSP00000427120.3:p.Asn200Ser
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.599A>G
  hgvsp: ENSP00000264773.2:p.Asn200Ser
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+40453A>G
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Asn200Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

5-113740152-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113740152
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113740152
    reference: chr 5
allele count: 2
allele frequency: 1.657138122462507e-5
allele num: 120690
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.600T>C
  hgvsp: ENST00000264773.3:c.600T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.600T>C
  hgvsp: ENST00000512097.3:c.600T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+40454T>C
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Asn200Asn
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ

5-113740170-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113740170
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113740170
    reference: chr 5
allele count: 3
allele frequency: 2.474675817467912e-5
allele num: 121228
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.618A>G
  hgvsp: ENST00000264773.3:c.618A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.618A>G
  hgvsp: ENST00000512097.3:c.618A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+40472A>G
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5668
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
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genotype quality: GenotypeQuality
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  bin: 8.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 4040
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg206Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum

5-113740185-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113740185
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113740185
    reference: chr 5
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.633T>C
  hgvsp: ENST00000264773.3:c.633T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.633T>C
  hgvsp: ENST00000512097.3:c.633T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+40487T>C
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9287
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 269
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 6.25e1
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genotype depth: GenotypeDepth
  all individuals: 342
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
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  variant carriers: 1
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3807
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Tyr211Tyr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

5-113740188-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113740188
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113740188
    reference: chr 5
allele count: 5
allele frequency: 4.120313143798929e-5
allele num: 121350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+40490G>A
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.636G>A
  hgvsp: ENST00000512097.3:c.636G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.636G>A
  hgvsp: ENST00000264773.3:c.636G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7989
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genotype depth: GenotypeDepth
  all individuals: 3693
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9288
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 2230
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 7.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 1291
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  variant carriers: 5
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 5
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  variant carriers: 0
hgvs: p.Glu212Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

5-113740190-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113740190
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113740190
    reference: chr 5
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+40492G>A
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.638G>A
  hgvsp: ENSP00000264773.2:p.Arg213His
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.638G>A
  hgvsp: ENSP00000427120.3:p.Arg213His
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7991
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 12
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hgvs: p.Arg213His
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/5-113740200-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113740200
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113740200
    reference: chr 5
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.648C>A
  hgvsp: ENSP00000427120.3:p.Phe216Leu
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+40502C>A
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.648C>A
  hgvsp: ENSP00000264773.2:p.Phe216Leu
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8341
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 2318
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Phe216Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

5-113740201-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113740201
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113740201
    reference: chr 5
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.649A>G
  hgvsp: ENSP00000264773.2:p.Ile217Val
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.649A>G
  hgvsp: ENSP00000427120.3:p.Ile217Val
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+40503A>G
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5664
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3589
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  variant carriers: 0
hgvs: p.Ile217Val
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

5-113740228-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113740228
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113740228
    reference: chr 5
allele count: 3
allele frequency: 2.471006852925672e-5
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.676A>G
  hgvsp: ENSP00000264773.2:p.Ile226Val
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+40530A>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.676A>G
  hgvsp: ENSP00000427120.3:p.Ile226Val
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3741
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  variant carriers: 0
hgvs: p.Ile226Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

5-113740251-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113740251
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113740251
    reference: chr 5
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+40553T>C
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.699T>C
  hgvsp: ENST00000512097.3:c.699T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.699T>C
  hgvsp: ENST00000264773.3:c.699T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Tyr233Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

5-113740252-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113740252
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113740252
    reference: chr 5
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+40554A>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.700A>G
  hgvsp: ENSP00000427120.3:p.Thr234Ala
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.700A>G
  hgvsp: ENSP00000264773.2:p.Thr234Ala
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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hgvs: p.Thr234Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

5-113740260-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 113740260
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 113740260
    reference: chr 5
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000427120
  ensembl transcript: ENST00000512097
  gene symbol: KCNN2
  hgvsc: ENST00000512097.3:c.708A>G
  hgvsp: ENST00000512097.3:c.708A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000080709
  ensembl transcript: ENST00000507750
  gene symbol: KCNN2
  hgvsc: ENST00000507750.1:n.251+40562A>G
  variant of: http://identifiers.org/hgnc/6291
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000080709
  ensembl protein: ENSP00000264773
  ensembl transcript: ENST00000264773
  gene symbol: KCNN2
  hgvsc: ENST00000264773.3:c.708A>G
  hgvsp: ENST00000264773.3:c.708A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6291
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7990
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8205
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9647
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5664
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3741
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4061
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12125
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3580
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2258
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3806
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2318
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr236Thr
num of homozygotes: 0
population: European (Non-Finnish)
reference allele: A

GenotypeQuality
all individuals: 116
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8494
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11336
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16152
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9666
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6386
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.568135486906069e-5
allele num: 63770
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.55e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.68e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.42e-1

DP
type: SiteQuality
SIO_000300: 1.386101e6

FS
type: SiteQuality
SIO_000300: 3.335e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

QD
type: SiteQuality
SIO_000300: 9.49e0

MQRankSum
type: SiteQuality
SIO_000300: -7.92e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.45e-1

GenotypeQuality
all individuals: 123
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15790
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.583581427757015e-5
allele num: 63148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6294
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.866820358219543e-5
allele num: 11278
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8430
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9522
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

DP
type: SiteQuality
SIO_000300: 1.364851e6

VQSLOD
type: SiteQuality
SIO_000300: 7.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.89e0

QD
type: SiteQuality
SIO_000300: 1.264e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQRankSum
type: SiteQuality
SIO_000300: 2.38e-1

FS
type: SiteQuality
SIO_000300: 5.509e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

GenotypeQuality
all individuals: 117
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62958
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6266
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15712
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.055520371543171e-4
allele num: 9474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11260
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

QD
type: SiteQuality
SIO_000300: 6.35e0

MQRankSum
type: SiteQuality
SIO_000300: -8.94e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.396e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.79e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.604e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.61e0

DP
type: SiteQuality
SIO_000300: 1.357837e6

GenotypeQuality
all individuals: 105
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.641443156823479e-5
allele num: 60922
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10998
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8950
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14750
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5950
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.342e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

FS
type: SiteQuality
SIO_000300: 1.328e0

MQ
type: SiteQuality
SIO_000300: 5.92e1

MQRankSum
type: SiteQuality
SIO_000300: -5.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.57e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.12e-1

DP
type: SiteQuality
SIO_000300: 1.286463e6

GenotypeQuality
all individuals: 448
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7970
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10730
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58880
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5698
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.165376898824878e-5
allele num: 13956
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.17e-1

DP
type: SiteQuality
SIO_000300: 1.225168e6

MQ
type: SiteQuality
SIO_000300: 5.766e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.447e0

VQSLOD
type: SiteQuality
SIO_000300: -2.608e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.41e-1

QD
type: SiteQuality
SIO_000300: 1.317e1

FS
type: SiteQuality
SIO_000300: 3.913e0

GenotypeQuality
all individuals: 355
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13956
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10730
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7970
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5698
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.698369565217391e-5
allele num: 58880
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.41e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.17e-1

FS
type: SiteQuality
SIO_000300: 3.913e0

VQSLOD
type: SiteQuality
SIO_000300: -2.608e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.447e0

MQ
type: SiteQuality
SIO_000300: 5.766e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

QD
type: SiteQuality
SIO_000300: 1.317e1

DP
type: SiteQuality
SIO_000300: 1.225168e6

GenotypeQuality
all individuals: 20850
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8988
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48922
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.524855138761818e-4
allele num: 6558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10942
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6976
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.94e-1

DP
type: SiteQuality
SIO_000300: 9.44354e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -7.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.29e-1

FS
type: SiteQuality
SIO_000300: 4.437e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.45e0

QD
type: SiteQuality
SIO_000300: 9.869999999999999e0

GenotypeQuality
all individuals: 39
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.139072847682119e-5
allele num: 48320
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6480
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4496
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10814
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6922
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8868
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.8e-3

DP
type: SiteQuality
SIO_000300: 9.25347e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.18e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.67e-1

QD
type: SiteQuality
SIO_000300: 1.6e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.4e0

GenotypeQuality
all individuals: 3640
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3990
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.631853785900783e-4
allele num: 6128
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5804
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43318
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7866
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.999999999999999e-3

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.345e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.766e0

DP
type: SiteQuality
SIO_000300: 7.95768e5

QD
type: SiteQuality
SIO_000300: 1.261e1

MQ
type: SiteQuality
SIO_000300: 5.903e1

GenotypeQuality
all individuals: 38
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 528
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7668
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.373718192176225e-5
allele num: 42128
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3892
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5940
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9290
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.31e-1

FS
type: SiteQuality
SIO_000300: 4.993e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.2e-2

QD
type: SiteQuality
SIO_000300: 1.312e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.85e-1

DP
type: SiteQuality
SIO_000300: 7.68235e5

GenotypeQuality
all individuals: 11
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.476668635558181e-4
allele num: 6772
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7948
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5038
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 464
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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European (Finnish)
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allele frequency: 0.0e0
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FS
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DP
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BaseQRankSum
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ReadPosRankSum
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QD
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ClippingRankSum
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MQ
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MQRankSum
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InbreedingCoeff
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VQSLOD
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele frequency: 3.052503052503053e-4
allele num: 3276
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European (Non-Finnish)
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allele frequency: 2.792672028596962e-5
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African
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South Asian
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Latino
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Other
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East Asian
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VQSLOD
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DP
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QD
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FS
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BaseQRankSum
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MQ
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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GenotypeQuality
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variant carriers: 3

Latino
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East Asian
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allele frequency: 0.0e0
allele num: 4886
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European (Finnish)
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allele frequency: 0.0e0
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Other
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African
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South Asian
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European (Non-Finnish)
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allele frequency: 1.117068811438785e-4
allele num: 35808
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BaseQRankSum
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VQSLOD
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QD
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FS
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MQ
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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variant carriers: 0

African
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European (Non-Finnish)
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allele count: 5
allele frequency: 1.509388395822013e-4
allele num: 33126
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
allele num: 3028
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Other
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allele frequency: 0.0e0
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East Asian
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Latino
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ReadPosRankSum
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BaseQRankSum
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DP
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QD
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MQ
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VQSLOD
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FS
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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East Asian
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European (Non-Finnish)
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allele frequency: 3.184307731499172e-5
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African
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Latino
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Other
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South Asian
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QD
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FS
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InbreedingCoeff
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BaseQRankSum
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MQ
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DP
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VQSLOD
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ClippingRankSum
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

Other
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African
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allele frequency: 1.452643811737362e-3
allele num: 3442
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Latino
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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MQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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MQ
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DP
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele frequency: 4.081299485756264e-5
allele num: 24502
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South Asian
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African
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Other
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East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
allele num: 4350
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European (Finnish)
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allele frequency: 0.0e0
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VQSLOD
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FS
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MQRankSum
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ClippingRankSum
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MQ
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QD
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DP
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele frequency: 0.0e0
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Latino
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African
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South Asian
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East Asian
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 4.600662495399337e-5
allele num: 21736
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DP
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ReadPosRankSum
type: SiteQuality
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FS
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VQSLOD
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MQ
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MQRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Other
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African
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 8.689607229753215e-5
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South Asian
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East Asian
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ReadPosRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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QD
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FS
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VQSLOD
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MQ
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MQRankSum
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ClippingRankSum
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European (Finnish)
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Latino
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European (Non-Finnish)
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allele frequency: 9.099733074496482e-5
allele num: 65936
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African
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East Asian
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Other
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South Asian
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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QD
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FS
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MQ
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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DP
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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European (Non-Finnish)
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African
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Latino
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South Asian
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Other
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East Asian
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MQRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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QD
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DP
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MQ
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GenotypeQuality
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East Asian
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African
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allele frequency: 8.719240457275722e-4
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European (Non-Finnish)
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European (Finnish)
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Other
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Latino
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South Asian
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DP
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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QD
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MQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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MQ
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GenotypeQuality
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South Asian
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African
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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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European (Non-Finnish)
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DP
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QD
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MQ
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FS
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BaseQRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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East Asian
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African
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Other
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Latino
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European (Finnish)
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South Asian
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European (Non-Finnish)
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MQRankSum
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ClippingRankSum
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QD
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FS
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MQ
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VQSLOD
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BaseQRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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SIO_000300: 9.09e-1

GenotypeQuality
all individuals: 4510
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506387081224391e-5
allele num: 66384
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16064
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.966e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.270234e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.067e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.520000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.246e0

QD
type: SiteQuality
SIO_000300: 1.05e1

MQRankSum
type: SiteQuality
SIO_000300: 1.66e0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16090
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Latino
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allele count: 1
allele frequency: 8.655011251514626e-5
allele num: 11554
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505978735580254e-5
allele num: 66402
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.925e0

VQSLOD
type: SiteQuality
SIO_000300: 3.71e0

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.271358e6

MQ
type: SiteQuality
SIO_000300: 5.747e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.44e-1

QD
type: SiteQuality
SIO_000300: 1.298e1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.011594639361542e-5
allele num: 66410
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 896
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

DP
type: SiteQuality
SIO_000300: 2.272563e6

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66498
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16278
num of homozygotes: 0

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.617e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.9e-2

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.931e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.14e-1

DP
type: SiteQuality
SIO_000300: 2.276841e6

QD
type: SiteQuality
SIO_000300: 9.51e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 3
allele frequency: 2.89073039121218e-4
allele num: 10378
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
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 (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66580
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.5163e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

DP
type: SiteQuality
SIO_000300: 2.282074e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.33e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.51e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.27e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.541e0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
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: 1.500960614793468e-5
allele num: 66624
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.799e0

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

MQ
type: SiteQuality
SIO_000300: 5.924e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.162e0

FS
type: SiteQuality
SIO_000300: 9.28e-1

QD
type: SiteQuality
SIO_000300: 1.37e1

DP
type: SiteQuality
SIO_000300: 2.28397e6

VQSLOD
type: SiteQuality
SIO_000300: 3.31e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

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

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 6.83e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.38e0

MQRankSum
type: SiteQuality
SIO_000300: 1.81e0

MQ
type: SiteQuality
SIO_000300: 5.944e1

FS
type: SiteQuality
SIO_000300: 9.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.06e-1

DP
type: SiteQuality
SIO_000300: 2.285355e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.57e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.461e0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

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

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

South Asian
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allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
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 count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.48e0

MQRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.966e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -8.113e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.098e0

DP
type: SiteQuality
SIO_000300: 2.285462e6

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499430216517723e-5
allele num: 66692
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

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

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.989e1

QD
type: SiteQuality
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MQRankSum
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeQuality
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bin: 9.75e1
variant carriers: 10

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

Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 1.155535012710885e-3
allele num: 8654
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
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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

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

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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QD
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.28673e6

FS
type: SiteQuality
SIO_000300: 1.092e0

MQRankSum
type: SiteQuality
SIO_000300: -1.45e-1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

South Asian
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allele frequency: 1.817080557238038e-4
allele num: 16510
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

South Asian
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num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.49947518368571e-5
allele num: 66690
num of homozygotes: 0

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

Latino
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allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
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DP
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

Latino
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num of homozygotes: 0

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

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

African
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Other
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

MQ
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InbreedingCoeff
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VQSLOD
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DP
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FS
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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QD
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

East Asian
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-1

FS
type: SiteQuality
SIO_000300: 8.986000000000001e0

QD
type: SiteQuality
SIO_000300: 1.143e1

VQSLOD
type: SiteQuality
SIO_000300: 3.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.187e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.38e-1

DP
type: SiteQuality
SIO_000300: 2.285649e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
all individuals: 19
bin: 3.75e1
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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 2.281e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.05e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.74e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.249e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.61e-1

DP
type: SiteQuality
SIO_000300: 2.285617e6

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
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: 10400
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.6e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.044e-1

FS
type: SiteQuality
SIO_000300: 4.707e0

QD
type: SiteQuality
SIO_000300: 1.34e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.91e-1

DP
type: SiteQuality
SIO_000300: 2.285624e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.381e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.273e0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 49
allele frequency: 7.349412047036238e-4
allele num: 66672
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.535833081342606e-4
allele num: 6614
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.335e1

VQSLOD
type: SiteQuality
SIO_000300: 5.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.09e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

MQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.15e-1

DP
type: SiteQuality
SIO_000300: 2.289306e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.64e-1

GenotypeQuality
all individuals: 3656
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66662
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: 3
allele frequency: 2.592016588906169e-4
allele num: 11574
num of homozygotes: 0

African
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allele count: 19
allele frequency: 1.826923076923077e-3
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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.068697657482704e-5
allele num: 16478
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.974e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

FS
type: SiteQuality
SIO_000300: 5.87e-1

QD
type: SiteQuality
SIO_000300: 1.196e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.805e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e-1

DP
type: SiteQuality
SIO_000300: 2.286844e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.64e0

MQRankSum
type: SiteQuality
SIO_000300: 2.68e-1

GenotypeQuality
all individuals: 15713
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500240038406145e-5
allele num: 66656
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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: 10400
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.2282e1

MQRankSum
type: SiteQuality
SIO_000300: 3.14e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.0e0

QD
type: SiteQuality
SIO_000300: 1.083e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.78e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.624e0

DP
type: SiteQuality
SIO_000300: 2.284551e6

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 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: 0
allele frequency: 0.0e0
allele num: 66632
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: 908
num of homozygotes: 0

East Asian
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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: 10402
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.089392278650591e-5
allele num: 16422
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.85e0

DP
type: SiteQuality
SIO_000300: 2.28159e6

QD
type: SiteQuality
SIO_000300: 1.44e1

VQSLOD
type: SiteQuality
SIO_000300: 4.94e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.04e-1

FS
type: SiteQuality
SIO_000300: 3.157e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.87e-1

MQ
type: SiteQuality
SIO_000300: 5.983e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.61e-1

GenotypeQuality
all individuals: 21219
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66632
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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16422
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.85e0

FS
type: SiteQuality
SIO_000300: 3.157e0

DP
type: SiteQuality
SIO_000300: 2.28159e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.983e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.94e-1

QD
type: SiteQuality
SIO_000300: 1.44e1

MQRankSum
type: SiteQuality
SIO_000300: -7.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.87e-1

GenotypeQuality
all individuals: 21219
bin: 9.75e1
variant carriers: 2

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66616
num of homozygotes: 0

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

Latino
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allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

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

East Asian
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allele count: 0
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allele num: 8654
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.42e-1

QD
type: SiteQuality
SIO_000300: 1.458e1

DP
type: SiteQuality
SIO_000300: 2.280488e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 8.090000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.15e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66596
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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.278728e6

MQRankSum
type: SiteQuality
SIO_000300: -1.889e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.011e0

QD
type: SiteQuality
SIO_000300: 1.887e1

FS
type: SiteQuality
SIO_000300: 5.620000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.35e-1

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.604e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502494140272853e-5
allele num: 66556
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.227e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.340000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.63e0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66554
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 904
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South Asian
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allele count: 0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.267316e6

VQSLOD
type: SiteQuality
SIO_000300: -1.647e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.0e-1

FS
type: SiteQuality
SIO_000300: 1.3022e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -4.25e-1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502674761074713e-5
allele num: 66548
num of homozygotes: 0

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

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

African
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allele count: 0
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allele num: 10400
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.94e-1

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.119e1

MQRankSum
type: SiteQuality
SIO_000300: 9.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.14e-1

FS
type: SiteQuality
SIO_000300: 7.224e0

VQSLOD
type: SiteQuality
SIO_000300: 2.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 6
allele frequency: 3.692307692307692e-4
allele num: 16250
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African
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allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.508837321149453e-5
allele num: 66536
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.42e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.11e0

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.516e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 2.258087e6

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
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African
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European (Non-Finnish)
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East Asian
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South Asian
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MQ
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QD
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BaseQRankSum
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MQRankSum
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DP
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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GenotypeQuality
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East Asian
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African
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Latino
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FS
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QD
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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DP
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MQ
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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European (Finnish)
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East Asian
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African
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South Asian
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DP
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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FS
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QD
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MQ
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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Other
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African
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Latino
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European (Finnish)
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East Asian
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DP
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ClippingRankSum
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QD
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ReadPosRankSum
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BaseQRankSum
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FS
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MQRankSum
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MQ
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VQSLOD
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GenotypeQuality
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European (Finnish)
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Latino
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African
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East Asian
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South Asian
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European (Non-Finnish)
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MQ
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FS
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VQSLOD
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QD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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DP
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ReadPosRankSum
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GenotypeQuality
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European (Finnish)
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African
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Other
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Latino
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European (Non-Finnish)
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South Asian
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East Asian
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MQ
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ReadPosRankSum
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MQRankSum
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DP
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ClippingRankSum
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FS
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InbreedingCoeff
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QD
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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European (Finnish)
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South Asian
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African
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European (Non-Finnish)
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Other
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East Asian
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Latino
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DP
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MQ
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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FS
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QD
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GenotypeQuality
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East Asian
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Other
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European (Finnish)
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African
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European (Non-Finnish)
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South Asian
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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QD
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VQSLOD
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DP
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MQ
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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South Asian
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European (Finnish)
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Latino
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African
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FS
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MQRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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DP
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ClippingRankSum
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QD
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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Latino
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East Asian
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African
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European (Finnish)
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DP
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ReadPosRankSum
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MQ
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FS
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InbreedingCoeff
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VQSLOD
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QD
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BaseQRankSum
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MQRankSum
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GenotypeQuality
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European (Non-Finnish)
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African
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European (Finnish)
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Latino
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East Asian
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South Asian
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FS
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DP
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BaseQRankSum
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MQ
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QD
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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GenotypeQuality
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Latino
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East Asian
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European (Non-Finnish)
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South Asian
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African
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MQ
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ReadPosRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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FS
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DP
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MQRankSum
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BaseQRankSum
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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South Asian
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African
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Latino
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QD
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InbreedingCoeff
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MQRankSum
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VQSLOD
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MQ
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FS
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DP
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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Latino
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European (Non-Finnish)
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African
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East Asian
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South Asian
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VQSLOD
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ClippingRankSum
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FS
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 2.461005e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.85e0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66464
num of homozygotes: 0

Latino
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allele frequency: 1.728309713100588e-4
allele num: 11572
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Other
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allele frequency: 0.0e0
allele num: 904
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6612
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South Asian
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allele frequency: 0.0e0
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.43e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.461e1

MQ
type: SiteQuality
SIO_000300: 5.963e1

GenotypeQuality
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variant carriers: 0

East Asian
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allele frequency: 0.0e0
allele num: 8654
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Latino
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allele frequency: 0.0e0
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African
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allele frequency: 9.609840476648087e-5
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Other
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.001200480192077e-5
allele num: 66640
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South Asian
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DP
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.555e1

MQRankSum
type: SiteQuality
SIO_000300: 1.58e0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499385252046661e-5
allele num: 66694
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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Other
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.976e1

FS
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SIO_000300: 1.816e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.6e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.470415e6

MQRankSum
type: SiteQuality
SIO_000300: -1.26e-1

QD
type: SiteQuality
SIO_000300: 1.348e1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66694
num of homozygotes: 0

Latino
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allele frequency: 4.319281271596407e-4
allele num: 11576
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European (Finnish)
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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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South Asian
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Other
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.965e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.21e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.04e-1

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.590000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.412e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.929999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.471137e6

VQSLOD
type: SiteQuality
SIO_000300: 4.67e-1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.49934029027228e-5
allele num: 66696
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South Asian
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

DP
type: SiteQuality
SIO_000300: 2.471008e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.93e0

GenotypeQuality
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variant carriers: 0

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

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

Other
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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South Asian
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BaseQRankSum
type: SiteQuality
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FS
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SIO_000300: 3.019e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.471383e6

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 8.88e-1

GenotypeQuality
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variant carriers: 0

East Asian
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Other
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African
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.289e0

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
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allele frequency: 1.498441620714457e-5
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East Asian
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Other
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Latino
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South Asian
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African
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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FS
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.984e1

VQSLOD
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.236e0

MQRankSum
type: SiteQuality
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DP
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

Other
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East Asian
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European (Finnish)
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South Asian
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allele num: 16512
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Latino
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African
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FS
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BaseQRankSum
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MQRankSum
type: SiteQuality
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DP
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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QD
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Latino
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num of homozygotes: 0

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

African
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European (Finnish)
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East Asian
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Other
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VQSLOD
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ReadPosRankSum
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MQ
type: SiteQuality
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DP
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FS
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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QD
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GenotypeQuality
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variant carriers: 1

European (Non-Finnish)
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num of homozygotes: 0