ClinVar Miner

List of variants in gene WNK1 reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (891):
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Gene type:
ClinVar version:
Total variants: 46
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HGVS dbSNP
NM_018979.3(WNK1):c.*1146G>A rs78913352
NM_018979.3(WNK1):c.*1986G>A rs2023944
NM_018979.3(WNK1):c.-203C>G rs72647363
NM_018979.3(WNK1):c.-452G>A rs118007973
NM_018979.3(WNK1):c.-91T>G rs3088353
NM_018979.3(WNK1):c.1287A>G (p.Ala429=) rs10774466
NM_018979.3(WNK1):c.1512A>G (p.Leu504=) rs56325964
NM_018979.3(WNK1):c.1526T>C (p.Ile509Thr) rs34728563
NM_018979.3(WNK1):c.2020A>G (p.Thr674Ala) rs11833299
NM_018979.3(WNK1):c.2052A>G (p.Ala684=) rs72648690
NM_018979.3(WNK1):c.2081T>C (p.Ile694Thr) rs61736905
NM_018979.3(WNK1):c.2206A>G (p.Ile736Val) rs147099510
NM_018979.3(WNK1):c.2328G>A (p.Gln776=) rs1012729
NM_018979.3(WNK1):c.2336C>T (p.Ala779Val) rs141428612
NM_018979.3(WNK1):c.2374-181C>T rs880054
NM_018979.3(WNK1):c.2490G>A (p.Pro830=) rs79816263
NM_018979.3(WNK1):c.2529G>A (p.Gln843=) rs9804992
NM_018979.3(WNK1):c.258T>C (p.Cys86=) rs3168640
NM_018979.3(WNK1):c.3166A>C (p.Thr1056Pro) rs956868
NM_018979.3(WNK1):c.3489+4C>T rs34032084
NM_018979.3(WNK1):c.3490-5T>A rs72650719
NM_018979.3(WNK1):c.3654A>G (p.Ser1218=) rs141971833
NM_018979.3(WNK1):c.4354A>G (p.Thr1452Ala) rs142543401
NM_018979.3(WNK1):c.446C>T (p.Ala149Val) rs34880640
NM_018979.3(WNK1):c.4517G>C (p.Cys1506Ser) rs7955371
NM_018979.3(WNK1):c.4605_4607delCAG (p.Ser1536del) rs567183841
NM_018979.3(WNK1):c.4983T>C (p.Ser1661=) rs149852592
NM_018979.3(WNK1):c.5281-4G>A rs72650740
NM_018979.3(WNK1):c.5284C>T (p.Leu1762=) rs72650741
NM_018979.3(WNK1):c.5397A>G (p.Gln1799=) rs148639270
NM_018979.3(WNK1):c.5424G>T (p.Met1808Ile) rs12828016
NM_018979.3(WNK1):c.5468C>T (p.Pro1823Leu) rs17755373
NM_018979.3(WNK1):c.5481A>G (p.Thr1827=) rs61736908
NM_018979.3(WNK1):c.5496G>A (p.Gln1832=) rs138219481
NM_018979.3(WNK1):c.5542_5550delACTAGTTCA (p.Thr1848_Ser1850del) rs544395150
NM_018979.3(WNK1):c.5991G>A (p.Glu1997=) rs61736907
NM_018979.3(WNK1):c.6828C>T (p.Tyr2276=) rs4766334
NM_018979.3(WNK1):c.684C>T (p.Gly228=) rs72647374
NM_018979.3(WNK1):c.759+16_759+18dupCTT rs398088143
NM_213655.4(WNK1):c.1401-11C>A rs11064573
NM_213655.4(WNK1):c.1479T>C (p.Asp493=) rs2286006
NM_213655.4(WNK1):c.1994C>T (p.Thr665Ile) rs2286007
NM_213655.4(WNK1):c.421G>A (p.Ala141Thr) rs11554421
NM_213655.4(WNK1):c.4716C>T (p.Asn1572=) rs7300444
NM_213655.4(WNK1):c.4800C>T (p.Thr1600=) rs10849577
NM_213655.4(WNK1):c.759+15A>C rs11064518

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