9-96030096-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030096
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030096
    reference: chr 9
allele count: 1
allele frequency: 1.034297298415457e-5
allele num: 96684
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2601C>T
  hgvsp: ENST00000349097.3:c.2601C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3765C>T
  hgvsp: ENST00000297954.4:c.3765C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1230C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2575C>T
  hgvsp: ENST00000411624.1:c.2575C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3752C>T
  hgvsp: ENST00000432730.1:c.3752C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1141C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.155C>T
  hgvsp: ENST00000448251.1:c.155C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3765C>T
  hgvsp: ENST00000395477.2:c.3765C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2601C>T
  hgvsp: ENST00000427277.2:c.2601C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000462595
  gene symbol: WNK2
  hgvsc: ENST00000462595.1:n.294C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.414C>T
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11751
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31709
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp1255Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/9-96030101-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030101
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030101
    reference: chr 9
allele count: 2
allele frequency: 2.034049996948925e-5
allele num: 98326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2606C>A
  hgvsp: ENSP00000297876.6:p.Ala869Glu
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3757C>A
  hgvsp: ENSP00000415038.1:p.Ala1253Glu
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2580C>A
  hgvsp: ENSP00000414622.1:p.Ala861Glu
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.160C>A
  hgvsp: ENSP00000390441.1:p.Ala54Glu
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1136C>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3770C>A
  hgvsp: ENSP00000378860.2:p.Ala1257Glu
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2606C>A
  hgvsp: ENSP00000411181.2:p.Ala869Glu
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3770C>A
  hgvsp: ENSP00000297954.4:p.Ala1257Glu
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.419C>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1235C>A
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10957
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala1257Glu
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

9-96030108-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030108
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030108
    reference: chr 9
allele count: 1
allele frequency: 1.000080006400512e-5
allele num: 99992
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2613C>T
  hgvsp: ENST00000349097.3:c.2613C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.426C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2613C>T
  hgvsp: ENST00000427277.2:c.2613C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1242C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3764C>T
  hgvsp: ENST00000432730.1:c.3764C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.167C>T
  hgvsp: ENST00000448251.1:c.167C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1129C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3777C>T
  hgvsp: ENST00000297954.4:c.3777C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3777C>T
  hgvsp: ENST00000395477.2:c.3777C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2587C>T
  hgvsp: ENST00000411624.1:c.2587C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6067
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 749
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp1259Asp
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

9-96030114-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030114
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030114
    reference: chr 9
allele count: 1
allele frequency: 9.928120408244311e-6
allele num: 100724
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2619C>T
  hgvsp: ENST00000427277.2:c.2619C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3770C>T
  hgvsp: ENST00000432730.1:c.3770C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1248C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1123C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2593C>T
  hgvsp: ENST00000411624.1:c.2593C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.432C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3783C>T
  hgvsp: ENST00000297954.4:c.3783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2619C>T
  hgvsp: ENST00000349097.3:c.2619C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.173C>T
  hgvsp: ENST00000448251.1:c.173C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3783C>T
  hgvsp: ENST00000395477.2:c.3783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7003
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29532
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9716
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3251
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2118
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu1261Leu
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum

9-96030115-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030115
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030115
    reference: chr 9
allele count: 1
allele frequency: 9.900009900009899e-6
allele num: 101010
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2594A>G
  hgvsp: ENSP00000414622.1:p.Ser866Gly
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3784A>G
  hgvsp: ENSP00000297954.4:p.Ser1262Gly
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.433A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1122A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2620A>G
  hgvsp: ENSP00000411181.2:p.Ser874Gly
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.174A>G
  hgvsp: ENSP00000390441.1:p.Ser59Gly
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3771A>G
  hgvsp: ENSP00000415038.1:p.Ser1258Gly
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3784A>G
  hgvsp: ENSP00000378860.2:p.Ser1262Gly
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2620A>G
  hgvsp: ENSP00000297876.6:p.Ser874Gly
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1249A>G
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9671
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7026
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2283
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser1262Gly
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

9-96030117-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030117
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030117
    reference: chr 9
allele count: 1
allele frequency: 9.900009900009899e-6
allele num: 101010
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1120C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.435C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3773C>T
  hgvsp: ENST00000432730.1:c.3773C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2622C>T
  hgvsp: ENST00000427277.2:c.2622C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2622C>T
  hgvsp: ENST00000349097.3:c.2622C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1251C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3786C>T
  hgvsp: ENST00000297954.4:c.3786C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.176C>T
  hgvsp: ENST00000448251.1:c.176C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2596C>T
  hgvsp: ENST00000411624.1:c.2596C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3786C>T
  hgvsp: ENST00000395477.2:c.3786C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9500
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3554
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28894
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7477
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7773
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1601
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser1262Ser
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

9-96030126-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030126
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030126
    reference: chr 9
allele count: 1
allele frequency: 9.862516519715171e-6
allele num: 101394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1260A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2631A>G
  hgvsp: ENST00000427277.2:c.2631A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2631A>G
  hgvsp: ENST00000349097.3:c.2631A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3795A>G
  hgvsp: ENST00000297954.4:c.3795A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3782A>G
  hgvsp: ENST00000432730.1:c.3782A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.444A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2605A>G
  hgvsp: ENST00000411624.1:c.2605A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.185A>G
  hgvsp: ENST00000448251.1:c.185A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1111A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3795A>G
  hgvsp: ENST00000395477.2:c.3795A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7266
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9653
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9274
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7210
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2802
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr1265Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

9-96030129-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030129
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030129
    reference: chr 9
allele count: 4
allele frequency: 3.951397806974217e-5
allele num: 101230
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2634C>T
  hgvsp: ENST00000349097.3:c.2634C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2608C>T
  hgvsp: ENST00000411624.1:c.2608C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1263C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2634C>T
  hgvsp: ENST00000427277.2:c.2634C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3798C>T
  hgvsp: ENST00000297954.4:c.3798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3785C>T
  hgvsp: ENST00000432730.1:c.3785C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3798C>T
  hgvsp: ENST00000395477.2:c.3798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1108C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.188C>T
  hgvsp: ENST00000448251.1:c.188C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.447C>T
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8324
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10036
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6910
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9248
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3437
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3140
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp1266Asp
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

9-96030132-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030132
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030132
    reference: chr 9
allele count: 1
allele frequency: 9.892175289346128e-6
allele num: 101090
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2611C>T
  hgvsp: ENST00000411624.1:c.2611C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3801C>T
  hgvsp: ENST00000297954.4:c.3801C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1105C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2637C>T
  hgvsp: ENST00000427277.2:c.2637C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.191C>T
  hgvsp: ENST00000448251.1:c.191C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3801C>T
  hgvsp: ENST00000395477.2:c.3801C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3788C>T
  hgvsp: ENST00000432730.1:c.3788C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.450C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2637C>T
  hgvsp: ENST00000349097.3:c.2637C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1266C>T
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9013
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1275
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala1267Ala
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

9-96030136-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030136
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030136
    reference: chr 9
allele count: 2
allele frequency: 1.980354879594423e-5
allele num: 100992
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.454C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2641C>T
  hgvsp: ENSP00000411181.2:p.Arg881Cys
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.195C>T
  hgvsp: ENSP00000390441.1:p.Arg66Cys
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2615C>T
  hgvsp: ENSP00000414622.1:p.Arg873Cys
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3792C>T
  hgvsp: ENSP00000415038.1:p.Arg1265Cys
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3805C>T
  hgvsp: ENSP00000297954.4:p.Arg1269Cys
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1270C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2641C>T
  hgvsp: ENSP00000297876.6:p.Arg881Cys
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3805C>T
  hgvsp: ENSP00000378860.2:p.Arg1269Cys
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1101C>T
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10722
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20484
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg1269Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

9-96030141-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030141
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030141
    reference: chr 9
allele count: 4
allele frequency: 3.95522683225883e-5
allele num: 101132
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2646C>T
  hgvsp: ENST00000349097.3:c.2646C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3797C>T
  hgvsp: ENST00000432730.1:c.3797C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.200C>T
  hgvsp: ENST00000448251.1:c.200C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3810C>T
  hgvsp: ENST00000297954.4:c.3810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2620C>T
  hgvsp: ENST00000411624.1:c.2620C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3810C>T
  hgvsp: ENST00000395477.2:c.3810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1275C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.459C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2646C>T
  hgvsp: ENST00000427277.2:c.2646C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1096C>T
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11627
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19239
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6059
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9060
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4064
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4344
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly1270Gly
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

9-96030143-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030143
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030143
    reference: chr 9
allele count: 1
allele frequency: 9.892762454987931e-6
allele num: 101084
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2622C>T
  hgvsp: ENSP00000414622.1:p.Ser875Phe
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2648C>T
  hgvsp: ENSP00000297876.6:p.Ser883Phe
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3799C>T
  hgvsp: ENSP00000415038.1:p.Ser1267Phe
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3812C>T
  hgvsp: ENSP00000297954.4:p.Ser1271Phe
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2648C>T
  hgvsp: ENSP00000411181.2:p.Ser883Phe
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1277C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.202C>T
  hgvsp: ENSP00000390441.1:p.Ser68Phe
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3812C>T
  hgvsp: ENSP00000378860.2:p.Ser1271Phe
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.461C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1094C>T
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18666
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9077
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4162
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser1271Phe
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

9-96030144-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030144
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030144
    reference: chr 9
allele count: 3
allele frequency: 2.977076510866329e-5
allele num: 100770
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2649C>T
  hgvsp: ENST00000427277.2:c.2649C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3813C>T
  hgvsp: ENST00000297954.4:c.3813C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1278C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3813C>T
  hgvsp: ENST00000395477.2:c.3813C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1093C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2623C>T
  hgvsp: ENST00000411624.1:c.2623C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.203C>T
  hgvsp: ENST00000448251.1:c.203C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2649C>T
  hgvsp: ENST00000349097.3:c.2649C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3800C>T
  hgvsp: ENST00000432730.1:c.3800C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.462C>T
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5956
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9070
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12387
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11213
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 904
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2095
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser1271Ser
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP

9-96030145-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030145
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030145
    reference: chr 9
allele count: 2
allele frequency: 1.99203187250996e-5
allele num: 100400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1092G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3801G>A
  hgvsp: ENSP00000415038.1:p.Asp1268Asn
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.463G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2650G>A
  hgvsp: ENSP00000411181.2:p.Asp884Asn
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.204G>A
  hgvsp: ENSP00000390441.1:p.Asp69Asn
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3814G>A
  hgvsp: ENSP00000378860.2:p.Asp1272Asn
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2624G>A
  hgvsp: ENSP00000414622.1:p.Asp876Asn
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2650G>A
  hgvsp: ENSP00000297876.6:p.Asp884Asn
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3814G>A
  hgvsp: ENSP00000297954.4:p.Asp1272Asn
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1279G>A
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9080
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17932
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12716
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3029
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asp1272Asn
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

9-96030161-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030161
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030161
    reference: chr 9
allele count: 11
allele frequency: 1.034184498514535e-4
allele num: 106364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.479C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3817C>T
  hgvsp: ENSP00000415038.1:p.Pro1273Leu
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2640C>T
  hgvsp: ENSP00000414622.1:p.Pro881Leu
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1076C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.220C>T
  hgvsp: ENSP00000390441.1:p.Pro74Leu
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2666C>T
  hgvsp: ENSP00000411181.2:p.Pro889Leu
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3830C>T
  hgvsp: ENSP00000378860.2:p.Pro1277Leu
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2666C>T
  hgvsp: ENSP00000297876.6:p.Pro889Leu
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1295C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3830C>T
  hgvsp: ENSP00000297954.4:p.Pro1277Leu
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22679
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6711
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31494
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro1277Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

9-96030162-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030162
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030162
    reference: chr 9
allele count: 2
allele frequency: 1.875152356128936e-5
allele num: 106658
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.480G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2641G>A
  hgvsp: ENST00000411624.1:c.2641G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2667G>A
  hgvsp: ENST00000349097.3:c.2667G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2667G>A
  hgvsp: ENST00000427277.2:c.2667G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3818G>A
  hgvsp: ENST00000432730.1:c.3818G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3831G>A
  hgvsp: ENST00000297954.4:c.3831G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3831G>A
  hgvsp: ENST00000395477.2:c.3831G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1075G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1296G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.221G>A
  hgvsp: ENST00000448251.1:c.221G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6540
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7932
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15353
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23389
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10707
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro1277Pro
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

9-96030166-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030166
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030166
    reference: chr 9
allele count: 2
allele frequency: 1.866228724992535e-5
allele num: 107168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.484C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.225C>T
  hgvsp: ENSP00000390441.1:p.His76Tyr
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1071C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2671C>T
  hgvsp: ENSP00000411181.2:p.His891Tyr
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3835C>T
  hgvsp: ENSP00000378860.2:p.His1279Tyr
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3822C>T
  hgvsp: ENSP00000415038.1:p.His1275Tyr
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3835C>T
  hgvsp: ENSP00000297954.4:p.His1279Tyr
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1300C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2645C>T
  hgvsp: ENSP00000414622.1:p.His883Tyr
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2671C>T
  hgvsp: ENSP00000297876.6:p.His891Tyr
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22849
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8435
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6452
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
hgvs: p.His1279Tyr
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

9-96030174-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030174
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030174
    reference: chr 9
allele count: 1
allele frequency: 9.298346753947148e-6
allele num: 107546
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3830C>G
  hgvsp: ENSP00000415038.1:p.Ser1277Arg
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1308C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.233C>G
  hgvsp: ENSP00000390441.1:p.Ser78Arg
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3843C>G
  hgvsp: ENSP00000297954.4:p.Ser1281Arg
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2653C>G
  hgvsp: ENSP00000414622.1:p.Ser885Arg
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.492C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2679C>G
  hgvsp: ENSP00000411181.2:p.Ser893Arg
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2679C>G
  hgvsp: ENSP00000297876.6:p.Ser893Arg
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1063C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3843C>G
  hgvsp: ENSP00000378860.2:p.Ser1281Arg
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8945
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1359
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 963
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ser1281Arg
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

9-96030178-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030178
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030178
    reference: chr 9
allele count: 3
allele frequency: 2.790749595341309e-5
allele num: 107498
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.237T>C
  hgvsp: ENSP00000390441.1:p.Cys80Arg
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3847T>C
  hgvsp: ENSP00000378860.2:p.Cys1283Arg
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2683T>C
  hgvsp: ENSP00000411181.2:p.Cys895Arg
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1059T>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.496T>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1312T>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3847T>C
  hgvsp: ENSP00000297954.4:p.Cys1283Arg
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3834T>C
  hgvsp: ENSP00000415038.1:p.Cys1279Arg
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2683T>C
  hgvsp: ENSP00000297876.6:p.Cys895Arg
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2657T>C
  hgvsp: ENSP00000414622.1:p.Cys887Arg
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Cys1283Arg
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

9-96030180-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030180
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030180
    reference: chr 9
allele count: 2
allele frequency: 1.862405482921742e-5
allele num: 107388
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3849C>G
  hgvsp: ENSP00000297954.4:p.Cys1283Trp
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3836C>G
  hgvsp: ENSP00000415038.1:p.Cys1279Trp
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1057C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3849C>G
  hgvsp: ENSP00000378860.2:p.Cys1283Trp
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2685C>G
  hgvsp: ENSP00000297876.6:p.Cys895Trp
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.239C>G
  hgvsp: ENSP00000390441.1:p.Cys80Trp
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2685C>G
  hgvsp: ENSP00000411181.2:p.Cys895Trp
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.498C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2659C>G
  hgvsp: ENSP00000414622.1:p.Cys887Trp
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1314C>G
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21850
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 994
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4274
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Cys1283Trp
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

9-96030180-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030180
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030180
    reference: chr 9
allele count: 5
allele frequency: 4.656013707304354e-5
allele num: 107388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2685C>T
  hgvsp: ENST00000427277.2:c.2685C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3849C>T
  hgvsp: ENST00000297954.4:c.3849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.498C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1314C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3836C>T
  hgvsp: ENST00000432730.1:c.3836C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2659C>T
  hgvsp: ENST00000411624.1:c.2659C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2685C>T
  hgvsp: ENST00000349097.3:c.2685C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.239C>T
  hgvsp: ENST00000448251.1:c.239C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1057C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3849C>T
  hgvsp: ENST00000395477.2:c.3849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6108
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21850
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13788
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Cys1283Cys
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

9-96030181-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030181
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030181
    reference: chr 9
allele count: 2
allele frequency: 1.856665428889714e-5
allele num: 107720
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3850G>A
  hgvsp: ENSP00000378860.2:p.Gly1284Ser
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3837G>A
  hgvsp: ENSP00000415038.1:p.Gly1280Ser
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3850G>A
  hgvsp: ENSP00000297954.4:p.Gly1284Ser
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.240G>A
  hgvsp: ENSP00000390441.1:p.Gly81Ser
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1056G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2686G>A
  hgvsp: ENSP00000297876.6:p.Gly896Ser
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2686G>A
  hgvsp: ENSP00000411181.2:p.Gly896Ser
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.499G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1315G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2660G>A
  hgvsp: ENSP00000414622.1:p.Gly888Ser
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4644
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6080
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13786
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9486
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly1284Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

9-96030185-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030185
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030185
    reference: chr 9
allele count: 4
allele frequency: 3.714572267003454e-5
allele num: 107684
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3854T>C
  hgvsp: ENSP00000378860.2:p.Leu1285Pro
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1052T>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2690T>C
  hgvsp: ENSP00000411181.2:p.Leu897Pro
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2690T>C
  hgvsp: ENSP00000297876.6:p.Leu897Pro
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3854T>C
  hgvsp: ENSP00000297954.4:p.Leu1285Pro
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1319T>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.244T>C
  hgvsp: ENSP00000390441.1:p.Leu82Pro
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3841T>C
  hgvsp: ENSP00000415038.1:p.Leu1281Pro
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.503T>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2664T>C
  hgvsp: ENSP00000414622.1:p.Leu889Pro
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5689
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20956
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6039
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10181
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11018
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu1285Pro
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD

9-96030192-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030192
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030192
    reference: chr 9
allele count: 2
allele frequency: 1.863689732933261e-5
allele num: 107314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.510C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2697C>T
  hgvsp: ENST00000427277.2:c.2697C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.251C>T
  hgvsp: ENST00000448251.1:c.251C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1326C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3861C>T
  hgvsp: ENST00000395477.2:c.3861C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1045C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2697C>T
  hgvsp: ENST00000349097.3:c.2697C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3848C>T
  hgvsp: ENST00000432730.1:c.3848C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3861C>T
  hgvsp: ENST00000297954.4:c.3861C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2671C>T
  hgvsp: ENST00000411624.1:c.2671C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20376
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6027
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6895
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10762
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1687
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr1287Thr
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

9-96030193-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030193
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030193
    reference: chr 9
allele count: 10
allele frequency: 9.32001192961527e-5
allele num: 107296
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3849G>A
  hgvsp: ENSP00000415038.1:p.Gly1284Arg
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3862G>A
  hgvsp: ENSP00000297954.4:p.Gly1288Arg
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.511G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3862G>A
  hgvsp: ENSP00000378860.2:p.Gly1288Arg
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1044G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.252G>A
  hgvsp: ENSP00000390441.1:p.Gly85Arg
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2672G>A
  hgvsp: ENSP00000414622.1:p.Gly892Arg
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2698G>A
  hgvsp: ENSP00000297876.6:p.Gly900Arg
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2698G>A
  hgvsp: ENSP00000411181.2:p.Gly900Arg
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1327G>A
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7148
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10860
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5994
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11684
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20240
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3651
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1173
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly1288Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

9-96030206-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030206
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030206
    reference: chr 9
allele count: 1
allele frequency: 9.252576842650678e-6
allele num: 108078
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1332+8T>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3867+8T>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3867+8T>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2677+8T>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1039+8T>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2703+8T>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.516+8T>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3854+8T>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.257+8T>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2703+8T>G
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9672
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18211
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11488
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5868
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1068
  bin: 5.25e1
  variant carriers: 0
hgvs: c.3867+8T>G
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

9-96030209-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030209
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030209
    reference: chr 9
allele count: 19
allele frequency: 1.761118217377602e-4
allele num: 107886
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1332+11G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1039+11G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3867+11G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3854+11G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2703+11G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.516+11G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.257+11G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2677+11G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3867+11G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2703+11G>A
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11021
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17208
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 11554
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10275
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5853
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 963
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4071
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2007
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

9-96030209-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030209
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030209
    reference: chr 9
allele count: 1
allele frequency: 9.269043249355801e-6
allele num: 107886
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.257+11G>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3854+11G>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1332+11G>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3867+11G>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2703+11G>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.516+11G>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3867+11G>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2677+11G>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2703+11G>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1039+11G>C
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10275
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11554
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5853
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11021
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 963
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4071
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1431
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

9-96030209-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030209
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030209
    reference: chr 9
allele count: 5
allele frequency: 4.634521624677901e-5
allele num: 107886
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2703+11G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.516+11G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.257+11G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3867+11G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2703+11G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3867+11G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2677+11G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3854+11G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1039+11G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1332+11G>T
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11021
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5853
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11554
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17208
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10275
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20098
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1035
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 4071
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5254
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

9-96030215-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030215
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030215
    reference: chr 9
allele count: 9
allele frequency: 8.380356444494106e-5
allele num: 107394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3854+17C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.516+17C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3867+17C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2703+17C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2703+17C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3867+17C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2677+17C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.257+17C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1332+17C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1039+17C>T
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12131
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16504
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9856
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11486
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1027
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 4884
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10698
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP

9-96030216-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030216
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030216
    reference: chr 9
allele count: 4
allele frequency: 3.721068690928034e-5
allele num: 107496
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1332+18G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2703+18G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.257+18G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3867+18G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.516+18G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1039+18G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2677+18G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2703+18G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3867+18G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3854+18G>A
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9669
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12484
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11467
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16339
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10657
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1133
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 685
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2825
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD

6-31979969-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31979969
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 31979969
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 2578
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000248290
  ensembl transcript: ENST00000507684
  gene symbol: TNXA
  hgvsc: ENST00000507684.1:n.281A>G
  variant of: http://identifiers.org/hgnc/11975
canonical: true
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6088
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3274
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5931
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3030
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 970
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 26
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 28
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 120
  num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD

9-96030219-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030219
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030219
    reference: chr 9
allele count: 1
allele frequency: 9.306481033391654e-6
allele num: 107452
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.516+21G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2703+21G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.257+21G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3867+21G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1039+21G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3867+21G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2703+21G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3854+21G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2677+21G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1332+21G>A
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5989
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11400
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12697
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2442
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 932
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10180
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ

9-96030225-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030225
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030225
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 107432
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2677+27G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.516+27G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3854+27G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3867+27G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2703+27G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.257+27G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1332+27G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3867+27G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2703+27G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1039+27G>T
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5977
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8895
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12552
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5762
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4149
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 670
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 1.25e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP

9-96030229-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030229
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030229
    reference: chr 9
allele count: 1
allele frequency: 9.29368029739777e-6
allele num: 107600
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2703+31G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3867+31G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.516+31G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1039+31G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1332+31G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3867+31G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2677+31G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2703+31G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.257+31G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3854+31G>T
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11421
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12417
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5834
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16940
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1148
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4088
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1108
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9597
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum

9-96030230-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030230
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030230
    reference: chr 9
allele count: 106136
allele frequency: 9.402884581310464e-1
allele num: 112876
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3867+32T>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2703+32T>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1039+32T>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.257+32T>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2703+32T>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3867+32T>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2677+32T>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3854+32T>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1332+32T>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.516+32T>C
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7170
  bin: 2.75e1
  variant carriers: 7067
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 155
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.25e1
  variant carriers: 408
genotype depth: GenotypeDepth
  all individuals: 10831
  bin: 1.25e1
  variant carriers: 10690
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 3.75e1
  variant carriers: 2334
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.75e1
  variant carriers: 535
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.75e1
  variant carriers: 301
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.25e1
  variant carriers: 697
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 4.75e1
  variant carriers: 997
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 237
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 2.5e0
  variant carriers: 257
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 4.25e1
  variant carriers: 1512
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 7.5e0
  variant carriers: 3236
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 151
genotype depth: GenotypeDepth
  all individuals: 14764
  bin: 1.75e1
  variant carriers: 14666
genotype depth: GenotypeDepth
  all individuals: 3955
  bin: 3.25e1
  variant carriers: 3916
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 132
genotype depth: GenotypeDepth
  all individuals: 11890
  bin: 2.25e1
  variant carriers: 11771
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.75e1
  variant carriers: 210
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 9.75e1
  variant carriers: 602
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 1.75e1
  variant carriers: 699
genotype quality: GenotypeQuality
  all individuals: 4306
  bin: 3.75e1
  variant carriers: 4274
genotype quality: GenotypeQuality
  all individuals: 5118
  bin: 4.75e1
  variant carriers: 5110
genotype quality: GenotypeQuality
  all individuals: 2553
  bin: 4.25e1
  variant carriers: 2545
num of homozygotes: 50169
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

9-96030231-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030231
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030231
    reference: chr 9
allele count: 12
allele frequency: 1.08782362752919e-4
allele num: 110312
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3867+33G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1332+33G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.257+33G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3867+33G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.516+33G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2677+33G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2703+33G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1039+33G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3854+33G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2703+33G>A
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8006
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15130
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14345
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7295
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1290
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1072
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5086
  bin: 9.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD

9-96030231-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030231
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030231
    reference: chr 9
allele count: 2
allele frequency: 1.813039379215317e-5
allele num: 110312
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3867+33G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3867+33G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.516+33G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2703+33G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3854+33G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2703+33G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1332+33G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.257+33G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2677+33G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1039+33G>T
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8006
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14345
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7619
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1782
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11928
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3118
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

9-96030238-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030238
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030238
    reference: chr 9
allele count: 1
allele frequency: 9.140934934825134e-6
allele num: 109398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2703+40C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3867+40C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3867+40C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1039+40C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.516+40C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2703+40C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2677+40C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3854+40C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.257+40C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1332+40C>G
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15548
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15023
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6046
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 837
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2671
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6076
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

9-96030242-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030242
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030242
    reference: chr 9
allele count: 1
allele frequency: 9.423827204704375e-6
allele num: 106114
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1332+44G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3854+44G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3867+44G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2677+44G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.257+44G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2703+44G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.516+44G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1039+44G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3867+44G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2703+44G>A
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14751
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5140
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15318
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9149
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8625
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1255
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2069
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

9-96030248-GCA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030248
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030246
    reference: chr 9
allele count: 53
allele frequency: 5.07769836555596e-4
allele num: 104378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2703+51_2703+52delCA
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1332+51_*1332+52delCA
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1039+51_-1039+52delCA
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.257+51_257+52delCA
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2703+51_2703+52delCA
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3867+51_3867+52delCA
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3867+51_3867+52delCA
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.516+51_516+52delCA
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2677+51_2677+52delCA
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3854+51_3854+52delCA
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14900
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5234
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15167
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5287
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 9080
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10017
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4009
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 7.25e1
  variant carriers: 2
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: GCA
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

9-96030248-GCAGGT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030248
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030243
    reference: chr 9
allele count: 19
allele frequency: 1.820306961237042e-4
allele num: 104378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2704-49_2703+51delCAGGT
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2678-49_2677+51delCAGGT
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2704-49_2703+51delCAGGT
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1038-49_-1039+51delCAGGT
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.517-49_516+51delCAGGT
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3868-49_3867+51delCAGGT
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3868-49_3867+51delCAGGT
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1332+51_*1333-49delCAGGT
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3855-49_3854+51delCAGGT
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.258-49_257+51delCAGGT
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5287
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9080
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14900
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3084
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3810
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10017
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 9.25e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: GCAGGT
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP

9-96030252-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030252
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030252
    reference: chr 9
allele count: 1
allele frequency: 1.055342141922411e-5
allele num: 94756
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1038-50G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3868-50G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2704-50G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.258-50G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3855-50G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2704-50G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3868-50G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1333-50G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.517-50G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2678-50G>A
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11827
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4227
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17454
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5879
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2284
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6903
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2276
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD

9-96030253-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030253
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030253
    reference: chr 9
allele count: 183
allele frequency: 2.14185393258427e-3
allele num: 85440
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3868-49T>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1333-49T>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3868-49T>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3855-49T>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2678-49T>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2704-49T>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1038-49T>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.517-49T>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2704-49T>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.258-49T>G
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3987
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 11760
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 17563
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6296
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 3.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 11718
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 4.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 4.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2085
  bin: 7.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 5215
  bin: 6.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 2777
  bin: 2.5e0
  variant carriers: 5
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

9-96030257-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030257
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030257
    reference: chr 9
allele count: 3
allele frequency: 3.326016097917914e-5
allele num: 90198
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2704-45C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3855-45C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.517-45C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1333-45C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2678-45C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3868-45C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1038-45C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3868-45C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2704-45C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.258-45C>G
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6683
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3720
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11102
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12565
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2743
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6143
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 890
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5027
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

9-96030258-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030258
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030258
    reference: chr 9
allele count: 682
allele frequency: 7.48841601335178e-3
allele num: 91074
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.517-44G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2704-44G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2704-44G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3868-44G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1038-44G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3868-44G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2678-44G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.258-44G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3855-44G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1333-44G>A
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17062
  bin: 1.25e1
  variant carriers: 204
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3766
  bin: 2.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 3.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 12617
  bin: 7.5e0
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 10640
  bin: 1.75e1
  variant carriers: 211
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7067
  bin: 2.25e1
  variant carriers: 96
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 16345
  bin: 2.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2084
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 685
  bin: 9.25e1
  variant carriers: 9
num of homozygotes: 11
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum

9-96030264-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030264
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030264
    reference: chr 9
allele count: 1
allele frequency: 1.096659574934749e-5
allele num: 91186
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.517-38G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1333-38G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2678-38G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2704-38G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2704-38G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3868-38G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.258-38G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3868-38G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1038-38G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3855-38G>A
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16765
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9439
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13004
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8264
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 910
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6128
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

9-96030267-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030267
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030267
    reference: chr 9
allele count: 1
allele frequency: 1.092036867164635e-5
allele num: 91572
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2704-35C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2704-35C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.258-35C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.517-35C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2678-35C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3868-35C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1333-35C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1038-35C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3868-35C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3855-35C>T
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8732
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9161
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13060
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9767
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17748
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1321
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

9-96030271-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030271
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030271
    reference: chr 9
allele count: 3
allele frequency: 3.262926627656566e-5
allele num: 91942
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.258-31G>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3868-31G>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2704-31G>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2704-31G>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3868-31G>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1038-31G>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3855-31G>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1333-31G>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.517-31G>C
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2678-31G>C
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7518
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 992
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 593
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18120
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum

9-96030272-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030272
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030272
    reference: chr 9
allele count: 1
allele frequency: 1.085564167697953e-5
allele num: 92118
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2678-30G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2704-30G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2704-30G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3855-30G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3868-30G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1038-30G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3868-30G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1333-30G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.258-30G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.517-30G>A
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15795
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4000
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1731
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1351
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

9-96030273-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030273
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030273
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 91944
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1333-29G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3855-29G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3868-29G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2704-29G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.517-29G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3868-29G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2704-29G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1038-29G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2678-29G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.258-29G>A
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 13188
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4039
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15663
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1717
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 833
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

9-96030273-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030273
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030273
    reference: chr 9
allele count: 2
allele frequency: 2.175237100843992e-5
allele num: 91944
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2678-29G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3868-29G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2704-29G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2704-29G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3855-29G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1333-29G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.517-29G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.258-29G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3868-29G>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1038-29G>T
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15663
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4039
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5536
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

9-96030277-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030277
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030277
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 92386
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1333-25A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3868-25A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.517-25A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2704-25A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3868-25A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3855-25A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2704-25A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1038-25A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2678-25A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.258-25A>G
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14885
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13236
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13170
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4186
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4240
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1784
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18283
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum

9-96030292-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030292
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030292
    reference: chr 9
allele count: 3
allele frequency: 3.200682812333298e-5
allele num: 93730
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3868-10C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3868-10C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1333-10C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3855-10C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2704-10C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1038-10C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2704-10C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2678-10C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.517-10C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.258-10C>T
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4224
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12979
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1000
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17887
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 798
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum

9-96030296-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030296
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030296
    reference: chr 9
allele count: 286
allele frequency: 3.035706704029211e-3
allele num: 94212
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.258-6A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3868-6A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2704-6A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3868-6A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2704-6A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1038-6A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1333-6A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3855-6A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.517-6A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2678-6A>G
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11282
  bin: 1.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 4972
  bin: 2.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 3736
  bin: 1.75e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12845
  bin: 7.5e0
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 19057
  bin: 2.25e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 1.25e1
  variant carriers: 0
hgvs: c.3868-6A>G
num of homozygotes: 4
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD

9-96030309-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030309
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030309
    reference: chr 9
allele count: 2
allele frequency: 2.095118374188142e-5
allele num: 95460
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2685G>A
  hgvsp: ENSP00000414622.1:p.Arg896Gln
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.265G>A
  hgvsp: ENSP00000390441.1:p.Arg89Gln
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3875G>A
  hgvsp: ENSP00000297954.4:p.Arg1292Gln
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3862G>A
  hgvsp: ENSP00000415038.1:p.Arg1288Gln
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2711G>A
  hgvsp: ENSP00000297876.6:p.Arg904Gln
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3875G>A
  hgvsp: ENSP00000378860.2:p.Arg1292Gln
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1031G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2711G>A
  hgvsp: ENSP00000411181.2:p.Arg904Gln
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1340G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.524G>A
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23032
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12230
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8777
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1086
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg1292Gln
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: G
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

9-96030316-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030316
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030316
    reference: chr 9
allele count: 1
allele frequency: 1.04887770086008e-5
allele num: 95340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2718C>T
  hgvsp: ENST00000349097.3:c.2718C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1024C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2692C>T
  hgvsp: ENST00000411624.1:c.2692C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3882C>T
  hgvsp: ENST00000297954.4:c.3882C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000165238
  ensembl transcript: ENST00000478583
  gene symbol: WNK2
  hgvsc: ENST00000478583.1:n.531C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3869C>T
  hgvsp: ENST00000432730.1:c.3869C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3882C>T
  hgvsp: ENST00000395477.2:c.3882C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2718C>T
  hgvsp: ENST00000427277.2:c.2718C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1347C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.272C>T
  hgvsp: ENST00000448251.1:c.272C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2192
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8626
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5838
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12431
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23318
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 572
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser1294Ser
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

9-96030324-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030324
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030324
    reference: chr 9
allele count: 1
allele frequency: 1.063807153039297e-5
allele num: 94002
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1016A>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2726A>G
  hgvsp: ENSP00000411181.2:p.Asn909Ser
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3890A>G
  hgvsp: ENSP00000297954.4:p.Asn1297Ser
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3890A>G
  hgvsp: ENSP00000378860.2:p.Asn1297Ser
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.280A>G
  hgvsp: ENSP00000390441.1:p.Asn94Ser
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3877A>G
  hgvsp: ENSP00000415038.1:p.Asn1293Ser
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2700A>G
  hgvsp: ENSP00000414622.1:p.Asn901Ser
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2726A>G
  hgvsp: ENSP00000297876.6:p.Asn909Ser
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1355A>G
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5910
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21686
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 747
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19124
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn1297Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: DP

9-96030325-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030325
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030325
    reference: chr 9
allele count: 3
allele frequency: 3.20855614973262e-5
allele num: 93500
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2727C>T
  hgvsp: ENST00000349097.3:c.2727C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1015C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.281C>T
  hgvsp: ENST00000448251.1:c.281C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3878C>T
  hgvsp: ENST00000432730.1:c.3878C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2701C>T
  hgvsp: ENST00000411624.1:c.2701C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2727C>T
  hgvsp: ENST00000427277.2:c.2727C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1356C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3891C>T
  hgvsp: ENST00000297954.4:c.3891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3891C>T
  hgvsp: ENST00000395477.2:c.3891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9661
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5947
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1896
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23668
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asn1297Asn
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

9-96030326-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030326
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030326
    reference: chr 9
allele count: 4
allele frequency: 4.295348137966582e-5
allele num: 93124
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2728G>A
  hgvsp: ENSP00000411181.2:p.Ala910Thr
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.282G>A
  hgvsp: ENSP00000390441.1:p.Ala95Thr
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2702G>A
  hgvsp: ENSP00000414622.1:p.Ala902Thr
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2728G>A
  hgvsp: ENSP00000297876.6:p.Ala910Thr
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3892G>A
  hgvsp: ENSP00000297954.4:p.Ala1298Thr
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3892G>A
  hgvsp: ENSP00000378860.2:p.Ala1298Thr
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1357G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3879G>A
  hgvsp: ENSP00000415038.1:p.Ala1294Thr
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1014G>A
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5957
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9900
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala1298Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

9-96030331-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030331
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030331
    reference: chr 9
allele count: 3
allele frequency: 3.281414070703535e-5
allele num: 91424
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2733C>T
  hgvsp: ENST00000427277.2:c.2733C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3897C>T
  hgvsp: ENST00000297954.4:c.3897C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1009C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3897C>T
  hgvsp: ENST00000395477.2:c.3897C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.287C>T
  hgvsp: ENST00000448251.1:c.287C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3884C>T
  hgvsp: ENST00000432730.1:c.3884C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1362C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2733C>T
  hgvsp: ENST00000349097.3:c.2733C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2707C>T
  hgvsp: ENST00000411624.1:c.2707C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18849
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11015
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5948
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 785
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 846
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21267
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro1299Pro
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/9-96030331-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030331
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030331
    reference: chr 9
allele count: 5
allele frequency: 5.469023451172558e-5
allele num: 91424
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1009C>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.287C>A
  hgvsp: ENST00000448251.1:c.287C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2733C>A
  hgvsp: ENST00000349097.3:c.2733C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1362C>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3884C>A
  hgvsp: ENST00000432730.1:c.3884C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2707C>A
  hgvsp: ENST00000411624.1:c.2707C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2733C>A
  hgvsp: ENST00000427277.2:c.2733C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3897C>A
  hgvsp: ENST00000297954.4:c.3897C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3897C>A
  hgvsp: ENST00000395477.2:c.3897C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18849
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5948
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11015
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1835
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21267
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1809
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21314
  bin: 2.25e1
  variant carriers: 1
hgvs: p.Pro1299Pro
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

9-96030334-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030334
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030334
    reference: chr 9
allele count: 2
allele frequency: 2.204634140964307e-5
allele num: 90718
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-1006G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2710G>A
  hgvsp: ENST00000411624.1:c.2710G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2736G>A
  hgvsp: ENST00000349097.3:c.2736G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3900G>A
  hgvsp: ENST00000395477.2:c.3900G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2736G>A
  hgvsp: ENST00000427277.2:c.2736G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3887G>A
  hgvsp: ENST00000432730.1:c.3887G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1365G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3900G>A
  hgvsp: ENST00000297954.4:c.3900G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.290G>A
  hgvsp: ENST00000448251.1:c.290G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11621
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18060
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14548
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val1300Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

9-96030346-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030346
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030346
    reference: chr 9
allele count: 1
allele frequency: 1.168115129427156e-5
allele num: 85608
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-994C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3912C>G
  hgvsp: ENSP00000378860.2:p.Asn1304Lys
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3899C>G
  hgvsp: ENSP00000415038.1:p.Asn1300Lys
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1377C>G
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2748C>G
  hgvsp: ENSP00000297876.6:p.Asn916Lys
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2722C>G
  hgvsp: ENSP00000414622.1:p.Asn908Lys
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2748C>G
  hgvsp: ENSP00000411181.2:p.Asn916Lys
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3912C>G
  hgvsp: ENSP00000297954.4:p.Asn1304Lys
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.302C>G
  hgvsp: ENSP00000390441.1:p.Asn101Lys
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16527
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12013
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4846
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15736
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asn1304Lys
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

9-96030346-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030346
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030346
    reference: chr 9
allele count: 26
allele frequency: 3.037099336510606e-4
allele num: 85608
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-994C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3899C>T
  hgvsp: ENST00000432730.1:c.3899C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1377C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3912C>T
  hgvsp: ENST00000395477.2:c.3912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3912C>T
  hgvsp: ENST00000297954.4:c.3912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2748C>T
  hgvsp: ENST00000427277.2:c.2748C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2748C>T
  hgvsp: ENST00000349097.3:c.2748C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2722C>T
  hgvsp: ENST00000411624.1:c.2722C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.302C>T
  hgvsp: ENST00000448251.1:c.302C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4846
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15736
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 16527
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12013
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27147
  bin: 2.25e1
  variant carriers: 0
hgvs: c.3912C>T
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

9-96030364-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030364
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030364
    reference: chr 9
allele count: 1
allele frequency: 1.285611436799342e-5
allele num: 77784
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2749+17C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2723+17C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3913+17C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-993+17C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1378+17C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2749+17C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3913+17C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.303+17C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3900+17C>T
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20928
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18476
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3169
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3732
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1262
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD

9-96030380-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030380
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030380
    reference: chr 9
allele count: 99
allele frequency: 1.564327023354296e-3
allele num: 63286
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2749+33C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3913+33C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2749+33C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-993+33C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1378+33C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.303+33C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2723+33C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3900+33C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3913+33C>T
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6448
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 17441
  bin: 1.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 21785
  bin: 7.5e0
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2358
  bin: 6.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1107
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22753
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 7.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 822
  bin: 8.25e1
  variant carriers: 7
num of homozygotes: 2
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum

9-96030384-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030384
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030384
    reference: chr 9
allele count: 4
allele frequency: 6.731287022078621e-5
allele num: 59424
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3900+37C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2749+37C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1378+37C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3913+37C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2749+37C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2723+37C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.303+37C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-993+37C>T
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3913+37C>T
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6687
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15747
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23443
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5121
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1097
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8116
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2070
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1753
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

9-96030385-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 96030385
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 96030385
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 58510
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000390441
  ensembl transcript: ENST00000448251
  gene symbol: WNK2
  hgvsc: ENST00000448251.1:c.303+38G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000414622
  ensembl transcript: ENST00000411624
  gene symbol: WNK2
  hgvsc: ENST00000411624.1:c.2723+38G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000411181
  ensembl transcript: ENST00000427277
  gene symbol: WNK2
  hgvsc: ENST00000427277.2:c.2749+38G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297954
  ensembl transcript: ENST00000297954
  gene symbol: WNK2
  hgvsc: ENST00000297954.4:c.3913+38G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378858
  ensembl transcript: ENST00000395475
  gene symbol: WNK2
  hgvsc: ENST00000395475.2:c.*1378+38G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000415038
  ensembl transcript: ENST00000432730
  gene symbol: WNK2
  hgvsc: ENST00000432730.1:c.3900+38G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000378860
  ensembl transcript: ENST00000395477
  gene symbol: WNK2
  hgvsc: ENST00000395477.2:c.3913+38G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000348347
  ensembl transcript: ENST00000356055
  gene symbol: WNK2
  hgvsc: ENST00000356055.3:c.-993+38G>A
  variant of: http://identifiers.org/hgnc/14542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165238
  ensembl protein: ENSP00000297876
  ensembl transcript: ENST00000349097
  gene symbol: WNK2
  hgvsc: ENST00000349097.3:c.2749+38G>A
  variant of: http://identifiers.org/hgnc/14542
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23876
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6716
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5416
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 905
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19798
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 693
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G

GenotypeQuality
all individuals: 131
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 905
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2776
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33774
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1534
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13636
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1597
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 883
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 392
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54284
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13070
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.249687578105474e-4
allele num: 8002
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4802
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7192
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.85e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.01e-1

DP
type: SiteQuality
SIO_000300: 1.169894e6

VQSLOD
type: SiteQuality
SIO_000300: -1.32e0

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

MQ
type: SiteQuality
SIO_000300: 5.899e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.57e0

GenotypeQuality
all individuals: 120
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 968
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1646
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1031
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1619
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13134
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 726
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2816
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33980
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 777
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 883
bin: 9.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13280
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8122
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7318
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8858
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 714
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.039151712887439e-4
allele num: 4904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.813894431344096e-5
allele num: 55130
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.79e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.214e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

QD
type: SiteQuality
SIO_000300: 2.18e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.517e0

DP
type: SiteQuality
SIO_000300: 1.179721e6

GenotypeQuality
all individuals: 631
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1871
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12820
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2856
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 947
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 884
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 196
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33736
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1919
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1148
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.786926843215039e-5
allele num: 55962
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7458
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8254
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 734
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9058
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4994
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.805e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.09e0

VQSLOD
type: SiteQuality
SIO_000300: -1.037e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.32e-1

DP
type: SiteQuality
SIO_000300: 1.18459e6

GenotypeQuality
all individuals: 863
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32351
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2305
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2817
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1476
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 443
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12940
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 945
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9168
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7498
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.203948952564411e-4
allele num: 8306
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5026
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56350
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.179256e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.168e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.363e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.43e-1

QD
type: SiteQuality
SIO_000300: 1.314e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.6496e1

MQRankSum
type: SiteQuality
SIO_000300: 6.35e-1

GenotypeQuality
all individuals: 753
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33266
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1414
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 344
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2104
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12940
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2864
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 723
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5046
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9208
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.770287494689137e-5
allele num: 56488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8334
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13686
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 742
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.25e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.183e0

VQSLOD
type: SiteQuality
SIO_000300: -1.135e0

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

FS
type: SiteQuality
SIO_000300: 3.597e0

MQ
type: SiteQuality
SIO_000300: 5.831e1

DP
type: SiteQuality
SIO_000300: 1.179647e6

QD
type: SiteQuality
SIO_000300: 1.443e1

GenotypeQuality
all individuals: 32225
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 659
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2455
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12978
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13678
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7498
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.769222603587984e-5
allele num: 56522
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5026
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8322
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.176782e6

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

VQSLOD
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SIO_000300: -1.257e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.66e-1

FS
type: SiteQuality
SIO_000300: 9.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.73e-1

QD
type: SiteQuality
SIO_000300: 7.88e0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5068
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9282
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13768
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.764290755116443e-5
allele num: 56680
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.34e-1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
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MQ
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VQSLOD
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BaseQRankSum
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QD
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InbreedingCoeff
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SIO_000300: -2.5e-3

ReadPosRankSum
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SIO_000300: 5.37e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

East Asian
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allele count: 1
allele frequency: 1.333688983728994e-4
allele num: 7498
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9244
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.534193320374625e-5
allele num: 56590
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13780
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5062
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.202501202501203e-4
allele num: 8316
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.132e0

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
SIO_000300: -5.3e-1

MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.124652e6

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.23e-1

QD
type: SiteQuality
SIO_000300: 1.252e1

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-2

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8296
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5034
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13804
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 742
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9242
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.770851779706039e-5
allele num: 56470
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.491e0

DP
type: SiteQuality
SIO_000300: 1.117507e6

FS
type: SiteQuality
SIO_000300: 8.929e0

MQRankSum
type: SiteQuality
SIO_000300: -1.535e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.19e-1

QD
type: SiteQuality
SIO_000300: 4.71e0

MQ
type: SiteQuality
SIO_000300: 5.906e1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.77355278093076e-5
allele num: 56384
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13826
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9246
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5018
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8270
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.331912626531699e-4
allele num: 7508
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

FS
type: SiteQuality
SIO_000300: 1.0849e1

DP
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -3.3e-3

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.942e1

VQSLOD
type: SiteQuality
SIO_000300: -1.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5060
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9292
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 56360
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East Asian
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allele count: 4
allele frequency: 5.326231691078562e-4
allele num: 7510
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South Asian
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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QD
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DP
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MQ
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MQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 1
allele frequency: 1.076889941847943e-4
allele num: 9286
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5062
num of homozygotes: 0

South Asian
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 56358
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African
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allele frequency: 0.0e0
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Other
type: Population
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ClippingRankSum
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QD
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BaseQRankSum
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FS
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DP
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MQ
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 2
allele frequency: 2.431906614785992e-4
allele num: 8224
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5036
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9272
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.780880467303035e-5
allele num: 56152
num of homozygotes: 0

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

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

African
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allele frequency: 1.222493887530562e-4
allele num: 8180
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.787182328341137e-5
allele num: 55954
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Other
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allele frequency: 0.0e0
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QD
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ReadPosRankSum
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SIO_000300: 7.84e-1

FS
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SIO_000300: 1.641e0

DP
type: SiteQuality
SIO_000300: 1.085539e6

ClippingRankSum
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SIO_000300: 9.22e-1

MQRankSum
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BaseQRankSum
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MQ
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SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

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

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

Other
type: Population
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.380662609871535e-5
allele num: 59160
num of homozygotes: 0

South Asian
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allele frequency: 6.262176454216532e-4
allele num: 14372
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East Asian
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ReadPosRankSum
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SIO_000300: 1.23e0

MQRankSum
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VQSLOD
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FS
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QD
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MQ
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SIO_000300: 6.0e1

BaseQRankSum
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ClippingRankSum
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SIO_000300: -8.93e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

DP
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SIO_000300: 1.273864e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele num: 10076
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South Asian
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allele num: 14384
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VQSLOD
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QD
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BaseQRankSum
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ReadPosRankSum
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DP
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MQ
type: SiteQuality
SIO_000300: 5.957e1

InbreedingCoeff
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FS
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MQRankSum
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ClippingRankSum
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SIO_000300: -6.879999999999999e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7898
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.356831151393085e-5
allele num: 59580
num of homozygotes: 0

South Asian
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allele num: 14452
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

VQSLOD
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MQRankSum
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FS
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SIO_000300: 8.034000000000001e0

QD
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.56e-1

MQ
type: SiteQuality
SIO_000300: 5.787e1

DP
type: SiteQuality
SIO_000300: 1.273363e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.46e-1

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

South Asian
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allele frequency: 6.890848952590959e-5
allele num: 14512
num of homozygotes: 0

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

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10204
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5672
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

MQ
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SIO_000300: 5.942e1

ClippingRankSum
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DP
type: SiteQuality
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ReadPosRankSum
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FS
type: SiteQuality
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MQRankSum
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BaseQRankSum
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VQSLOD
type: SiteQuality
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QD
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SIO_000300: 1.121e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

African
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allele frequency: 3.449068751437112e-4
allele num: 8698
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.350083752093803e-5
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South Asian
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African
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European (Finnish)
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Other
type: Population
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QD
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InbreedingCoeff
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MQ
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FS
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MQRankSum
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ReadPosRankSum
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VQSLOD
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DP
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.350083752093803e-5
allele num: 59700
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European (Finnish)
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Other
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East Asian
type: Population
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South Asian
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allele frequency: 2.073255010366275e-4
allele num: 14470
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

FS
type: SiteQuality
SIO_000300: 1.226e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.61e0

MQRankSum
type: SiteQuality
SIO_000300: -1.64e-1

DP
type: SiteQuality
SIO_000300: 1.254162e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.66e-1

QD
type: SiteQuality
SIO_000300: 1.386e1

GenotypeQuality
all individuals: 1040
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4346
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29001
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3202
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3030
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10893
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 940
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1178
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 547
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1834
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 990
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14538
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.788566953797964e-5
allele num: 10216
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7908
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.147052076164258e-4
allele num: 8718
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59840
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5702
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

FS
type: SiteQuality
SIO_000300: 7.403e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

DP
type: SiteQuality
SIO_000300: 1.252981e6

VQSLOD
type: SiteQuality
SIO_000300: -8.309999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.49e0

QD
type: SiteQuality
SIO_000300: 1.326e1

MQ
type: SiteQuality
SIO_000300: 5.962e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.59e-1

GenotypeQuality
all individuals: 977
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1238
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1167
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 876
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2276
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 970
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 291
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1167
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27089
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3321
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4219
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3677
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8702
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5694
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59872
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7908
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.919263178522438e-4
allele num: 10206
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.79e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.23e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.07e0

DP
type: SiteQuality
SIO_000300: 1.23637e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

QD
type: SiteQuality
SIO_000300: 1.515e1

GenotypeQuality
all individuals: 948
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4194
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3943
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24718
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3606
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2763
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1107
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10988
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1443
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 972
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1117
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.15233924867481e-4
allele num: 8678
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7888
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10158
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14446
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5672
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.675603217158177e-5
allele num: 59680
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.217707e6

QD
type: SiteQuality
SIO_000300: 1.03e1

FS
type: SiteQuality
SIO_000300: 4.857e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.06e-1

GenotypeQuality
all individuals: 2860
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1689
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 954
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 984
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 318
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4253
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1149
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1131
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1437
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10974
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23945
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3960
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 215
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 7
allele frequency: 8.05523590333717e-4
allele num: 8690
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.028157683024939e-5
allele num: 59664
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7864
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5670
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10156
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14462
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

QD
type: SiteQuality
SIO_000300: 1.292e1

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.612e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

DP
type: SiteQuality
SIO_000300: 1.214666e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 236
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11095
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4999
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3937
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1555
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 954
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22614
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1131
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3913
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3940
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1533
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1014
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14548
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7928
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8812
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.664946222237022e-5
allele num: 60062
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5720
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

DP
type: SiteQuality
SIO_000300: 1.192908e6

QD
type: SiteQuality
SIO_000300: 1.788e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

GenotypeQuality
all individuals: 1824
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4480
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1035
bin: 9.75e1
variant carriers: 17

GenotypeQuality
all individuals: 1431
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5254
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1126
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20098
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 528
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1063
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3758
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10913
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.137138958380714e-4
allele num: 8794
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5742
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 3.003504088102787e-4
allele num: 59930
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.183876e6

MQRankSum
type: SiteQuality
SIO_000300: -1.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.34e-1

FS
type: SiteQuality
SIO_000300: 1.745e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.14e0

QD
type: SiteQuality
SIO_000300: 1.143e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

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

GenotypeQuality
all individuals: 119
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2007
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3758
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1063
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1824
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4480
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10913
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1126
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5254
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1035
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 532
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20098
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5742
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.668613382279326e-5
allele num: 59930
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8794
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14516
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

FS
type: SiteQuality
SIO_000300: 1.745e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.34e-1

QD
type: SiteQuality
SIO_000300: 1.143e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.14e0

DP
type: SiteQuality
SIO_000300: 1.183876e6

GenotypeQuality
all individuals: 2007
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3758
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1063
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4480
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10913
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1824
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1431
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 963
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1126
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 8.343066911396629e-5
allele num: 59930
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5742
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8794
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14516
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7906
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.183876e6

VQSLOD
type: SiteQuality
SIO_000300: 2.14e0

MQRankSum
type: SiteQuality
SIO_000300: -1.02e-1

FS
type: SiteQuality
SIO_000300: 1.745e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

QD
type: SiteQuality
SIO_000300: 1.143e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.34e-1

GenotypeQuality
all individuals: 558
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2176
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 9.25e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10180
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14466
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5676
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 6.849315068493151e-4
allele num: 8760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.675434775324197e-5
allele num: 59686
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.549069589599796e-4
allele num: 7846
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

MQRankSum
type: SiteQuality
SIO_000300: 3.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-2

FS
type: SiteQuality
SIO_000300: 9.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.128e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.06e-1

DP
type: SiteQuality
SIO_000300: 1.1786e6

GenotypeQuality
all individuals: 585
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1034
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variant carriers: 4

GenotypeQuality
all individuals: 523
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10192
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8796
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7848
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.380452788514633e-4
allele num: 14488
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5704
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.35098183767844e-5
allele num: 59684
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.5e-2

DP
type: SiteQuality
SIO_000300: 1.176006e6

MQRankSum
type: SiteQuality
SIO_000300: 1.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.846e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.31e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.211e1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1284
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1036
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.08e-2

DP
type: SiteQuality
SIO_000300: 6.7465e4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.286e0

MQ
type: SiteQuality
SIO_000300: 3.781e1

QD
type: SiteQuality
SIO_000300: 1.436e1

GenotypeQuality
all individuals: 1030
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 122
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 567
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variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5704
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.909894969596462e-5
allele num: 14472
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8770
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59716
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10166
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7840
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.228e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.32e0

MQRankSum
type: SiteQuality
SIO_000300: 1.49e-1

DP
type: SiteQuality
SIO_000300: 1.169192e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

QD
type: SiteQuality
SIO_000300: 9.81e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 4388
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9866
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1151
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GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5471
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1028
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5688
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7832
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8840
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59688
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14480
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

QD
type: SiteQuality
SIO_000300: 2.57e0

VQSLOD
type: SiteQuality
SIO_000300: -2.857e0

MQRankSum
type: SiteQuality
SIO_000300: 7.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.99e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.171447e6

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 2930
bin: 5.25e1
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GenotypeQuality
all individuals: 268
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7856
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10144
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.672688344707614e-5
allele num: 59784
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8854
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5668
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14506
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.177252e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.68e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.792e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.93e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.63e-1

GenotypeQuality
all individuals: 1235
bin: 2.75e1
variant carriers: 1200

GenotypeQuality
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bin: 9.25e1
variant carriers: 1622

GenotypeQuality
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bin: 5.75e1
variant carriers: 2669

GenotypeQuality
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bin: 2.25e1
variant carriers: 1392

GenotypeQuality
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variant carriers: 2288

GenotypeQuality
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GenotypeQuality
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variant carriers: 1128

GenotypeQuality
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variant carriers: 108

GenotypeQuality
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variant carriers: 216

GenotypeQuality
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variant carriers: 5505

GenotypeQuality
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bin: 9.75e1
variant carriers: 14400

GenotypeQuality
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bin: 7.75e1
variant carriers: 2902

GenotypeQuality
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variant carriers: 4605

GenotypeQuality
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variant carriers: 1858

GenotypeQuality
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bin: 3.25e1
variant carriers: 3056

GenotypeQuality
all individuals: 4060
bin: 6.75e1
variant carriers: 4018

South Asian
type: Population
allele count: 14838
allele frequency: 9.581557535838822e-1
allele num: 15486
num of homozygotes: 7109

Latino
type: Population
allele count: 10383
allele frequency: 9.732845894263217e-1
allele num: 10668
num of homozygotes: 5053

Other
type: Population
allele count: 800
allele frequency: 9.66183574879227e-1
allele num: 828
num of homozygotes: 386

European (Non-Finnish)
type: Population
allele count: 59422
allele frequency: 9.540491940145142e-1
allele num: 62284
num of homozygotes: 28334

African
type: Population
allele count: 6612
allele frequency: 7.074684356944148e-1
allele num: 9346
num of homozygotes: 2337

East Asian
type: Population
allele count: 8166
allele frequency: 9.997551420176298e-1
allele num: 8168
num of homozygotes: 4082

European (Finnish)
type: Population
allele count: 5915
allele frequency: 9.703083989501312e-1
allele num: 6096
num of homozygotes: 2868

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.45e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.440023e6

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-2

QD
type: SiteQuality
SIO_000300: 3.204e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.071e-1

GenotypeQuality
all individuals: 1782
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7619
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GenotypeQuality
all individuals: 502
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9254
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5892
num of homozygotes: 0

Latino
type: Population
allele count: 12
allele frequency: 1.154290111581377e-3
allele num: 10396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7954
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15088
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

DP
type: SiteQuality
SIO_000300: 1.371987e6

MQ
type: SiteQuality
SIO_000300: 5.919e1

VQSLOD
type: SiteQuality
SIO_000300: 5.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.065e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.28e-1

FS
type: SiteQuality
SIO_000300: 3.189e0

MQRankSum
type: SiteQuality
SIO_000300: 2.19e-1

QD
type: SiteQuality
SIO_000300: 1.188e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5086
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 502
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GenotypeQuality
all individuals: 706
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GenotypeQuality
all individuals: 4784
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GenotypeQuality
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GenotypeQuality
all individuals: 881
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GenotypeQuality
all individuals: 1720
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1290
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7954
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9254
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.325556733828208e-4
allele num: 15088
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60908
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.19e-1

FS
type: SiteQuality
SIO_000300: 3.189e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.28e-1

MQ
type: SiteQuality
SIO_000300: 5.919e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.065e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

DP
type: SiteQuality
SIO_000300: 1.371987e6

VQSLOD
type: SiteQuality
SIO_000300: 5.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.188e1

GenotypeQuality
all individuals: 638
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12359
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1242
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2230
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 854
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 695
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5065
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9158
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5840
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.654588173003739e-5
allele num: 60438
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14990
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.262e0

DP
type: SiteQuality
SIO_000300: 1.350621e6

VQSLOD
type: SiteQuality
SIO_000300: -9.354e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.0834e1

QD
type: SiteQuality
SIO_000300: 1.256e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

GenotypeQuality
all individuals: 5146
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1667
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 716
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 793
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variant carriers: 0

GenotypeQuality
all individuals: 1438
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.143118427069044e-4
allele num: 8748
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14898
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5480
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7710
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9992
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58534
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.447e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.62e0

QD
type: SiteQuality
SIO_000300: 1.217e1

DP
type: SiteQuality
SIO_000300: 1.337927e6

VQSLOD
type: SiteQuality
SIO_000300: -6.298e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.02e-1

MQ
type: SiteQuality
SIO_000300: 5.844e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.09e-1

GenotypeQuality
all individuals: 3084
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1632
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 1351
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2921
bin: 4.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1726
bin: 6.75e1
variant carriers: 4

GenotypeQuality
all individuals: 8420
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1035
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4908
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
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variant carriers: 5

GenotypeQuality
all individuals: 634
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 781
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 3810
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 6858
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2498
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4693
bin: 9.75e1
variant carriers: 23

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14728
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 33
allele frequency: 5.72042712522535e-4
allele num: 57688
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 10
allele frequency: 1.874765654293213e-3
allele num: 5334
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7544
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 1.155802126675913e-3
allele num: 8652
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.236e0

VQSLOD
type: SiteQuality
SIO_000300: -1.513e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.555e0

QD
type: SiteQuality
SIO_000300: 2.48e0

DP
type: SiteQuality
SIO_000300: 1.335324e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

MQ
type: SiteQuality
SIO_000300: 5.384e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.36e0

FS
type: SiteQuality
SIO_000300: 1.10198e2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.433e0

GenotypeQuality
all individuals: 760
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2498
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2921
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4693
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 1632
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6858
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 370
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8420
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1351
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4009
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4908
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 781
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1726
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1035
bin: 7.75e1
variant carriers: 2

African
type: Population
allele count: 6
allele frequency: 6.934812760055479e-4
allele num: 8652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 736
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14728
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.874765654293213e-4
allele num: 5334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 2.080155318263764e-4
allele num: 57688
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.433e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.555e0

FS
type: SiteQuality
SIO_000300: 1.10198e2

VQSLOD
type: SiteQuality
SIO_000300: -1.513e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.36e0

MQRankSum
type: SiteQuality
SIO_000300: -1.236e0

QD
type: SiteQuality
SIO_000300: 2.48e0

MQ
type: SiteQuality
SIO_000300: 5.384e1

DP
type: SiteQuality
SIO_000300: 1.335324e6

GenotypeQuality
all individuals: 4322
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14596
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1115
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variant carriers: 0

GenotypeQuality
all individuals: 345
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variant carriers: 0

GenotypeQuality
all individuals: 5451
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variant carriers: 0

GenotypeQuality
all individuals: 1392
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variant carriers: 0

GenotypeQuality
all individuals: 2832
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 537
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GenotypeQuality
all individuals: 1690
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variant carriers: 0

GenotypeQuality
all individuals: 819
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variant carriers: 0

GenotypeQuality
all individuals: 688
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variant carriers: 0

GenotypeQuality
all individuals: 599
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variant carriers: 0

GenotypeQuality
all individuals: 5248
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variant carriers: 0

GenotypeQuality
all individuals: 1800
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 828
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1014
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.407407407407407e-5
allele num: 13500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6834
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4778
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7850
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52486
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.08e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.46e0

DP
type: SiteQuality
SIO_000300: 1.131559e6

VQSLOD
type: SiteQuality
SIO_000300: -4.509e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.371e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.69e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.599e1

GenotypeQuality
all individuals: 6023
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2002
bin: 5.25e1
variant carriers: 8

GenotypeQuality
all individuals: 13797
bin: 2.25e1
variant carriers: 5

GenotypeQuality
all individuals: 4798
bin: 2.75e1
variant carriers: 12

GenotypeQuality
all individuals: 899
bin: 5.75e1
variant carriers: 12

GenotypeQuality
all individuals: 2042
bin: 1.25e1
variant carriers: 10

GenotypeQuality
all individuals: 2381
bin: 4.25e1
variant carriers: 11

GenotypeQuality
all individuals: 771
bin: 7.75e1
variant carriers: 11

GenotypeQuality
all individuals: 4954
bin: 3.75e1
variant carriers: 12

GenotypeQuality
all individuals: 2909
bin: 4.75e1
variant carriers: 8

GenotypeQuality
all individuals: 451
bin: 8.75e1
variant carriers: 9

GenotypeQuality
all individuals: 3221
bin: 1.75e1
variant carriers: 9

GenotypeQuality
all individuals: 1337
bin: 6.75e1
variant carriers: 8

GenotypeQuality
all individuals: 557
bin: 9.25e1
variant carriers: 8

GenotypeQuality
all individuals: 3098
bin: 9.75e1
variant carriers: 60

GenotypeQuality
all individuals: 660
bin: 8.25e1
variant carriers: 7

Other
type: Population
allele count: 2
allele frequency: 3.436426116838488e-3
allele num: 582
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.316829075585989e-4
allele num: 7594
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 136
allele frequency: 4.002354326074161e-2
allele num: 3398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 41
allele frequency: 8.565936820992812e-4
allele num: 47864
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12850
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6136
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 4.27594070695553e-4
allele num: 7016
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

FS
type: SiteQuality
SIO_000300: 6.7256e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.85e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.594e0

MQRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

QD
type: SiteQuality
SIO_000300: 8.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.09e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

VQSLOD
type: SiteQuality
SIO_000300: -2.133e1

DP
type: SiteQuality
SIO_000300: 1.099686e6

GenotypeQuality
all individuals: 508
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 7.75e1
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GenotypeQuality
all individuals: 1372
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 15516
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6353
bin: 3.25e1
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GenotypeQuality
all individuals: 2341
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GenotypeQuality
all individuals: 1664
bin: 7.5e0
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GenotypeQuality
all individuals: 1570
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variant carriers: 0

GenotypeQuality
all individuals: 5112
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GenotypeQuality
all individuals: 654
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GenotypeQuality
all individuals: 2270
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 701
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variant carriers: 1

GenotypeQuality
all individuals: 3745
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1577
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7536
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 7.208073041806823e-4
allele num: 4162
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8112
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 638
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6468
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13094
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.71e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.6e-3

MQ
type: SiteQuality
SIO_000300: 5.845e1

DP
type: SiteQuality
SIO_000300: 1.098973e6

MQRankSum
type: SiteQuality
SIO_000300: -8.93e-1

QD
type: SiteQuality
SIO_000300: 5.64e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.085e0

VQSLOD
type: SiteQuality
SIO_000300: -3.233e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.736e0

GenotypeQuality
all individuals: 1575
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5041
bin: 2.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1610
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7385
bin: 6.25e1
variant carriers: 5

GenotypeQuality
all individuals: 1207
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 2423
bin: 4.75e1
variant carriers: 5

GenotypeQuality
all individuals: 4860
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 240
bin: 5.75e1
variant carriers: 9

GenotypeQuality
all individuals: 537
bin: 8.75e1
variant carriers: 11

GenotypeQuality
all individuals: 822
bin: 8.25e1
variant carriers: 11

GenotypeQuality
all individuals: 1076
bin: 5.25e1
variant carriers: 12

GenotypeQuality
all individuals: 981
bin: 7.75e1
variant carriers: 13

GenotypeQuality
all individuals: 1622
bin: 6.75e1
variant carriers: 6

GenotypeQuality
all individuals: 6155
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 7.25e1
variant carriers: 16

GenotypeQuality
all individuals: 4548
bin: 9.75e1
variant carriers: 619

South Asian
type: Population
allele count: 25
allele frequency: 1.903456677326024e-3
allele num: 13134
num of homozygotes: 0

Other
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allele count: 6
allele frequency: 9.230769230769232e-3
allele num: 650
num of homozygotes: 0

African
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allele count: 237
allele frequency: 3.142402545743835e-2
allele num: 7542
num of homozygotes: 5

European (Finnish)
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allele count: 6
allele frequency: 1.323918799646955e-3
allele num: 4532
num of homozygotes: 0

Latino
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allele count: 24
allele frequency: 2.9296875e-3
allele num: 8192
num of homozygotes: 1

East Asian
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allele count: 355
allele frequency: 5.454824830977259e-2
allele num: 6508
num of homozygotes: 5

European (Non-Finnish)
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allele count: 29
allele frequency: 5.740755404228363e-4
allele num: 50516
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.402e1

FS
type: SiteQuality
SIO_000300: 5.21e-1

MQRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 1.13e-2

ClippingRankSum
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VQSLOD
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ReadPosRankSum
type: SiteQuality
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DP
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SIO_000300: 1.104831e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

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

Other
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allele frequency: 0.0e0
allele num: 658
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 50646
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4556
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 7.675775253300584e-5
allele num: 13028
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: -4.98e-1

VQSLOD
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MQRankSum
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DP
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InbreedingCoeff
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MQ
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BaseQRankSum
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FS
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SIO_000300: 4.117e0

ClippingRankSum
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QD
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SIO_000300: 1.24e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 6512
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7578
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 1.21036068748487e-4
allele num: 8262
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 50922
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 658
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4584
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.47e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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InbreedingCoeff
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QD
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DP
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BaseQRankSum
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SIO_000300: -3.742e0

MQRankSum
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ClippingRankSum
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SIO_000300: -8.100000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 2

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13086
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7594
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8354
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 51096
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4612
num of homozygotes: 0

East Asian
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allele count: 3
allele frequency: 4.592774035517453e-4
allele num: 6532
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 668
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.721e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.17e-1

DP
type: SiteQuality
SIO_000300: 1.134641e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -6.34e-1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

VQSLOD
type: SiteQuality
SIO_000300: -8.194e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4608
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 51190
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.311303435615001e-4
allele num: 7626
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8382
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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ClippingRankSum
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QD
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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DP
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SIO_000300: 1.13761e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

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

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

East Asian
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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Latino
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Other
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South Asian
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European (Non-Finnish)
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allele frequency: 3.913741145160659e-5
allele num: 51102
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FS
type: SiteQuality
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MQ
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QD
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VQSLOD
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DP
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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European (Non-Finnish)
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African
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Latino
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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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MQ
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QD
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VQSLOD
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FS
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ClippingRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Finnish)
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13048
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.835679490621763e-5
allele num: 52142
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.93e-1

QD
type: SiteQuality
SIO_000300: 1.363e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e-1

MQ
type: SiteQuality
SIO_000300: 5.865e1

VQSLOD
type: SiteQuality
SIO_000300: -1.398e0

DP
type: SiteQuality
SIO_000300: 1.202597e6

FS
type: SiteQuality
SIO_000300: 6.949e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.982e0

GenotypeQuality
all individuals: 4227
bin: 9.75e1
variant carriers: 259

GenotypeQuality
all individuals: 1035
bin: 7.75e1
variant carriers: 5

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 6

GenotypeQuality
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bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 653
bin: 4.25e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1910
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 874
bin: 7.25e1
variant carriers: 2

GenotypeQuality
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bin: 8.25e1
variant carriers: 6

GenotypeQuality
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bin: 2.25e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1995
bin: 6.75e1
variant carriers: 5

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 543
bin: 8.75e1
variant carriers: 4

GenotypeQuality
all individuals: 3003
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 8
allele frequency: 9.203865623561896e-4
allele num: 8692
num of homozygotes: 0

African
type: Population
allele count: 275
allele frequency: 3.491620111731843e-2
allele num: 7876
num of homozygotes: 4

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6690
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.730221186537801e-5
allele num: 52354
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13052
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4858
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.18e0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.113e0

DP
type: SiteQuality
SIO_000300: 1.221374e6

QD
type: SiteQuality
SIO_000300: 1.282e1

GenotypeQuality
all individuals: 697
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2087
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 904
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5024
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6764
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.770028275212064e-5
allele num: 53050
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7998
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12988
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 5.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.168e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.679999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.654e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.46e-1

DP
type: SiteQuality
SIO_000300: 1.264585e6

GenotypeQuality
all individuals: 17455
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4027
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 465
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 76
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variant carriers: 0

GenotypeQuality
all individuals: 1849
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 859
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variant carriers: 0

GenotypeQuality
all individuals: 25700
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variant carriers: 0

GenotypeQuality
all individuals: 233
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variant carriers: 0

GenotypeQuality
all individuals: 1035
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6734
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8054
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 724
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.889859016517368e-5
allele num: 52914
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8918
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5054
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12942
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.883e1

MQRankSum
type: SiteQuality
SIO_000300: 5.38e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.318e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

DP
type: SiteQuality
SIO_000300: 1.267185e6

QD
type: SiteQuality
SIO_000300: 2.169e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.003e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e-1

GenotypeQuality
all individuals: 4027
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1016
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
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variant carriers: 0

GenotypeQuality
all individuals: 452
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variant carriers: 0

GenotypeQuality
all individuals: 860
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variant carriers: 0

GenotypeQuality
all individuals: 1863
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variant carriers: 0

GenotypeQuality
all individuals: 463
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variant carriers: 0

GenotypeQuality
all individuals: 248
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variant carriers: 0

GenotypeQuality
all individuals: 253
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variant carriers: 0

GenotypeQuality
all individuals: 24182
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variant carriers: 0

GenotypeQuality
all individuals: 542
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variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1699
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variant carriers: 0

GenotypeQuality
all individuals: 894
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variant carriers: 0

GenotypeQuality
all individuals: 695
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8756
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12786
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.917839745310882e-5
allele num: 52142
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5024
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.201e0

MQRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e0

VQSLOD
type: SiteQuality
SIO_000300: -2.988e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.54e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.82e1

QD
type: SiteQuality
SIO_000300: 6.79e0

DP
type: SiteQuality
SIO_000300: 1.248264e6

GenotypeQuality
all individuals: 267
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1709
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 756
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variant carriers: 0

GenotypeQuality
all individuals: 19382
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variant carriers: 0

GenotypeQuality
all individuals: 1968
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variant carriers: 0

GenotypeQuality
all individuals: 66
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GenotypeQuality
all individuals: 4028
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 883
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GenotypeQuality
all individuals: 489
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variant carriers: 0

GenotypeQuality
all individuals: 889
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variant carriers: 0

GenotypeQuality
all individuals: 856
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8694
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51866
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.792667509481669e-4
allele num: 7910
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4992
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12746
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.245342e6

VQSLOD
type: SiteQuality
SIO_000300: 3.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.23e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

QD
type: SiteQuality
SIO_000300: 1.077e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.340000000000001e-1

GenotypeQuality
all individuals: 851
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 300
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variant carriers: 0

GenotypeQuality
all individuals: 153
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variant carriers: 0

GenotypeQuality
all individuals: 1923
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 765
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variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 2.311604253351826e-4
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.874617381533573e-5
allele num: 51618
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7890
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12724
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4976
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 710
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.055e1

FS
type: SiteQuality
SIO_000300: 2.747e0

DP
type: SiteQuality
SIO_000300: 1.241047e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.1e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e-1

GenotypeQuality
all individuals: 994
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 695
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 708
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6344
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4920
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.848127244740893e-4
allele num: 7796
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50606
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12590
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.218078e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.31e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.7e-2

MQ
type: SiteQuality
SIO_000300: 5.884e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.17e-1

FS
type: SiteQuality
SIO_000300: 2.604e0

QD
type: SiteQuality
SIO_000300: 1.067e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.32e-1

GenotypeQuality
all individuals: 349
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 994
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variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 180
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variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 785
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 539
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GenotypeQuality
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bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 4028
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 846
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8460
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.942811755361398e-5
allele num: 12590
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6344
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African
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allele frequency: 1.282709081580298e-4
allele num: 7796
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 5.928150812156662e-5
allele num: 50606
num of homozygotes: 0

FS
type: SiteQuality
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DP
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InbreedingCoeff
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MQ
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SIO_000300: 5.884e1

ClippingRankSum
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BaseQRankSum
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VQSLOD
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MQRankSum
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4862
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 6298
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 50170
num of homozygotes: 0

Latino
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allele frequency: 2.385496183206107e-4
allele num: 8384
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 7738
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12558
num of homozygotes: 0

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

VQSLOD
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SIO_000300: -2.236e0

FS
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MQRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -3.0e-3

MQ
type: SiteQuality
SIO_000300: 5.799e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e-1

DP
type: SiteQuality
SIO_000300: 1.204686e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.93e-1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4590
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7346
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5848
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12146
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.297016861219196e-4
allele num: 7710
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47282
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.894e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.118628e6

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47282
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7346
num of homozygotes: 0

South Asian
type: Population
allele count: 18
allele frequency: 1.481969372632966e-3
allele num: 12146
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5848
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 1.037613488975357e-3
allele num: 7710
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.029e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.118628e6

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e0

FS
type: SiteQuality
SIO_000300: 1.894e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e-1

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5132
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6818
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4294
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.703220191470844e-5
allele num: 11490
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42636
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.983e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.89e-1

InbreedingCoeff
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MQRankSum
type: SiteQuality
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QD
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 5076
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 3.90625e-3
allele num: 512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 37
allele frequency: 1.081239041496201e-3
allele num: 34220
num of homozygotes: 0

African
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allele count: 2
allele frequency: 3.489183531053733e-4
allele num: 5732
num of homozygotes: 0

European (Finnish)
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allele count: 52
allele frequency: 1.394849785407725e-2
allele num: 3728
num of homozygotes: 2

South Asian
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allele count: 2
allele frequency: 1.947419668938656e-4
allele num: 10270
num of homozygotes: 0

East Asian
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allele count: 4
allele frequency: 1.067235859124867e-3
allele num: 3748
num of homozygotes: 0

FS
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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MQ
type: SiteQuality
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QD
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.58e-2

DP
type: SiteQuality
SIO_000300: 8.84789e5

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.244536030972898e-5
allele num: 32028
num of homozygotes: 0

East Asian
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South Asian
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allele count: 2
allele frequency: 1.997602876548142e-4
allele num: 10012
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Other
type: Population
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allele frequency: 0.0e0
allele num: 494
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3508
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3468
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 31514
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South Asian
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