ClinVar Miner

List of variants in gene WNK4 studied for abdominal and pelvic region disorder

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 61
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HGVS dbSNP
NM_032387.5(WNK4):c.*335C>G rs61755636
NM_032387.5(WNK4):c.*340C>A rs886052954
NM_032387.5(WNK4):c.*6G>A rs61755635
NM_032387.5(WNK4):c.-22C>T rs200318202
NM_032387.5(WNK4):c.1339G>A (p.Asp447Asn) rs566923583
NM_032387.5(WNK4):c.1477-13A>G rs61754357
NM_032387.5(WNK4):c.14C>T (p.Pro5Leu) rs577125376
NM_032387.5(WNK4):c.1523G>A (p.Arg508His) rs55997156
NM_032387.5(WNK4):c.1524T>C (p.Arg508=) rs55879206
NM_032387.5(WNK4):c.1572G>T (p.Leu524=) rs144084546
NM_032387.5(WNK4):c.1574G>A (p.Arg525His) rs200182836
NM_032387.5(WNK4):c.1641C>T (p.Ala547=) rs9916754
NM_032387.5(WNK4):c.1653C>T (p.Pro551=) rs55751736
NM_032387.5(WNK4):c.1664C>G (p.Pro555Arg) rs57737815
NM_032387.5(WNK4):c.1679A>G (p.Glu560Gly) rs193922734
NM_032387.5(WNK4):c.1682C>T (p.Pro561Leu) rs193922735
NM_032387.5(WNK4):c.1684G>A (p.Glu562Lys) rs137853093
NM_032387.5(WNK4):c.1690G>C (p.Asp564His) rs193922736
NM_032387.5(WNK4):c.1691A>C (p.Asp564Ala) rs137853094
NM_032387.5(WNK4):c.1693C>G (p.Gln565Glu) rs137853092
NM_032387.5(WNK4):c.16G>A (p.Ala6Thr) rs61754324
NM_032387.5(WNK4):c.1719C>T (p.His573=) rs56243382
NM_032387.5(WNK4):c.1801G>T (p.Ala601Ser) rs55781437
NM_032387.5(WNK4):c.1809G>A (p.Gln603=) rs768020150
NM_032387.5(WNK4):c.1827A>G (p.Pro609=) rs201340788
NM_032387.5(WNK4):c.1853G>T (p.Cys618Phe) rs143396070
NM_032387.5(WNK4):c.1864-11T>C rs61755599
NM_032387.5(WNK4):c.1885C>T (p.Arg629Cys) rs61755600
NM_032387.5(WNK4):c.1888T>C (p.Ser630Pro) rs56030257
NM_032387.5(WNK4):c.1953C>T (p.Ser651=) rs766220456
NM_032387.5(WNK4):c.2005C>T (p.Arg669Trp) rs769815091
NM_032387.5(WNK4):c.2207G>A (p.Arg736Gln) rs149389156
NM_032387.5(WNK4):c.2213G>A (p.Arg738Gln) rs200823152
NM_032387.5(WNK4):c.2334C>T (p.Leu778=) rs61755621
NM_032387.5(WNK4):c.2369C>A (p.Thr790Asn) rs56227191
NM_032387.5(WNK4):c.239C>A (p.Ala80Asp) rs61754326
NM_032387.5(WNK4):c.2474C>T (p.Pro825Leu) rs56226218
NM_032387.5(WNK4):c.2476G>A (p.Gly826Ser) rs190384194
NM_032387.5(WNK4):c.2588T>G (p.Leu863Arg) rs545588214
NM_032387.5(WNK4):c.2672C>T (p.Thr891Met) rs56081375
NM_032387.5(WNK4):c.2724G>A (p.Pro908=) rs2290042
NM_032387.5(WNK4):c.2823G>A (p.Leu941=) rs371107660
NM_032387.5(WNK4):c.2837C>G (p.Pro946Arg) rs200187290
NM_032387.5(WNK4):c.2842C>A (p.Leu948Ile) rs372807256
NM_032387.5(WNK4):c.2881C>T (p.Pro961Ser) rs2290041
NM_032387.5(WNK4):c.2900C>G (p.Pro967Arg) rs775923469
NM_032387.5(WNK4):c.3022+3A>G rs146903073
NM_032387.5(WNK4):c.3074C>T (p.Pro1025Leu) rs56099549
NM_032387.5(WNK4):c.3251T>C (p.Val1084Ala) rs148648427
NM_032387.5(WNK4):c.3505A>G (p.Lys1169Glu) rs193922737
NM_032387.5(WNK4):c.3518C>A (p.Pro1173Gln) rs117902541
NM_032387.5(WNK4):c.3523A>G (p.Ile1175Val) rs761259011
NM_032387.5(WNK4):c.3553C>T (p.Arg1185Cys) rs137853095
NM_032387.5(WNK4):c.3595C>A (p.Arg1199Ser) rs200519604
NM_032387.5(WNK4):c.3610C>T (p.Arg1204Cys) rs56116165
NM_032387.5(WNK4):c.3659G>T (p.Gly1220Val) rs756125712
NM_032387.5(WNK4):c.47C>T (p.Thr16Ile) rs61754325
NM_032387.5(WNK4):c.507C>A (p.Pro169=) rs61754328
NM_032387.5(WNK4):c.679G>T (p.Gly227Trp) rs140897013
NM_032387.5(WNK4):c.717G>T (p.Ser239=) rs765644398
NM_032387.5(WNK4):c.945C>T (p.Gly315=) rs61754348

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