ClinVar Miner

List of variants in gene WNK1 reported as uncertain significance for Hereditary sensory and autonomic neuropathy type IIA; Pseudohypoaldosteronism type 2C

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 109
Download table as spreadsheet
HGVS dbSNP
NC_000012.12:g.(?_753546)_(871368_?)dup
NC_000012.12:g.(?_753546)_(878381_?)dup
NC_000012.12:g.(?_753546)_(908812_?)dup
NM_018979.3(WNK1):c.1269G>A (p.Ser423=) rs955095527
NM_018979.3(WNK1):c.1277A>G (p.Gln426Arg)
NM_018979.3(WNK1):c.128C>G (p.Ala43Gly)
NM_018979.3(WNK1):c.1669G>A (p.Ala557Thr)
NM_018979.3(WNK1):c.1787C>T (p.Ser596Phe)
NM_018979.3(WNK1):c.1823C>G (p.Ser608Cys) rs1455320237
NM_018979.3(WNK1):c.1855A>G (p.Thr619Ala) rs149388376
NM_018979.3(WNK1):c.2021C>T (p.Thr674Ile) rs1249953042
NM_018979.3(WNK1):c.2092G>A (p.Val698Ile) rs764336343
NM_018979.3(WNK1):c.2092G>C (p.Val698Leu) rs764336343
NM_018979.3(WNK1):c.2105C>A (p.Ser702Tyr) rs772771448
NM_018979.3(WNK1):c.2134A>G (p.Ser712Gly)
NM_018979.3(WNK1):c.214A>G (p.Thr72Ala) rs1483871160
NM_018979.3(WNK1):c.217A>G (p.Thr73Ala) rs1038270127
NM_018979.3(WNK1):c.2188G>A (p.Val730Ile)
NM_018979.3(WNK1):c.2266C>G (p.Gln756Glu)
NM_018979.3(WNK1):c.2290A>G (p.Thr764Ala) rs143890340
NM_018979.3(WNK1):c.2320G>A (p.Val774Met) rs144292256
NM_018979.3(WNK1):c.2441C>T (p.Ser814Leu) rs199930107
NM_018979.3(WNK1):c.2468A>G (p.His823Arg) rs56015776
NM_018979.3(WNK1):c.2489C>T (p.Pro830Leu) rs575889688
NM_018979.3(WNK1):c.2558C>T (p.Thr853Met) rs766223909
NM_018979.3(WNK1):c.2567C>A (p.Thr856Lys)
NM_018979.3(WNK1):c.2642C>T (p.Thr881Ile) rs183506727
NM_018979.3(WNK1):c.2656C>G (p.Pro886Ala)
NM_018979.3(WNK1):c.2684A>G (p.Gln895Arg) rs200100184
NM_018979.3(WNK1):c.2899G>A (p.Ala967Thr) rs1555146635
NM_018979.3(WNK1):c.2942C>T (p.Pro981Leu)
NM_018979.3(WNK1):c.2947G>C (p.Glu983Gln)
NM_018979.3(WNK1):c.3029T>C (p.Val1010Ala) rs769099133
NM_018979.3(WNK1):c.3068T>C (p.Leu1023Ser) rs766021155
NM_018979.3(WNK1):c.3133G>T (p.Val1045Phe)
NM_018979.3(WNK1):c.314C>G (p.Pro105Arg) rs142165599
NM_018979.3(WNK1):c.3188C>T (p.Thr1063Ile) rs201379287
NM_018979.3(WNK1):c.3209G>C (p.Ser1070Thr) rs760251215
NM_018979.3(WNK1):c.3314C>G (p.Ser1105Cys) rs767286874
NM_018979.3(WNK1):c.3326G>A (p.Arg1109His) rs750478389
NM_018979.3(WNK1):c.3573G>C (p.Met1191Ile) rs1555148491
NM_018979.3(WNK1):c.3592G>A (p.Val1198Met) rs1478319114
NM_018979.3(WNK1):c.3614G>A (p.Gly1205Glu)
NM_018979.3(WNK1):c.3623G>T (p.Ser1208Ile) rs972194980
NM_018979.3(WNK1):c.3659C>T (p.Ser1220Phe)
NM_018979.3(WNK1):c.3859G>T (p.Ala1287Ser) rs149186881
NM_018979.3(WNK1):c.385G>T (p.Ala129Ser) rs752345591
NM_018979.3(WNK1):c.3883T>C (p.Ser1295Pro) rs1555149377
NM_018979.3(WNK1):c.3884C>G (p.Ser1295Cys)
NM_018979.3(WNK1):c.3932G>T (p.Arg1311Ile) rs773117623
NM_018979.3(WNK1):c.3991C>A (p.Pro1331Thr)
NM_018979.3(WNK1):c.3991C>T (p.Pro1331Ser)
NM_018979.3(WNK1):c.4043C>T (p.Thr1348Ile) rs746601991
NM_018979.3(WNK1):c.4055C>T (p.Ala1352Val)
NM_018979.3(WNK1):c.4058C>T (p.Thr1353Ile) rs1182500229
NM_018979.3(WNK1):c.4108G>A (p.Val1370Ile)
NM_018979.3(WNK1):c.413C>T (p.Pro138Leu) rs1277355342
NM_018979.3(WNK1):c.4231A>T (p.Ser1411Cys) rs761892301
NM_018979.3(WNK1):c.4328C>G (p.Ser1443Cys)
NM_018979.3(WNK1):c.4336G>A (p.Ala1446Thr) rs376176091
NM_018979.3(WNK1):c.4388G>A (p.Ser1463Asn) rs757201529
NM_018979.3(WNK1):c.4474G>A (p.Val1492Ile) rs774954731
NM_018979.3(WNK1):c.4484C>G (p.Thr1495Ser) rs760474824
NM_018979.3(WNK1):c.4547C>A (p.Pro1516His) rs1454330405
NM_018979.3(WNK1):c.4703A>C (p.His1568Pro)
NM_018979.3(WNK1):c.4792C>T (p.Pro1598Ser)
NM_018979.3(WNK1):c.4816C>G (p.Pro1606Ala)
NM_018979.3(WNK1):c.4823C>T (p.Ala1608Val)
NM_018979.3(WNK1):c.4925C>T (p.Thr1642Ile) rs1555150817
NM_018979.3(WNK1):c.511C>T (p.Leu171Phe)
NM_018979.3(WNK1):c.5144A>G (p.Asn1715Ser) rs756614581
NM_018979.3(WNK1):c.515_517delTGG (p.Val172del)
NM_018979.3(WNK1):c.5189C>T (p.Thr1730Ile) rs375562377
NM_018979.3(WNK1):c.5221A>G (p.Thr1741Ala)
NM_018979.3(WNK1):c.5258A>G (p.Lys1753Arg) rs752078094
NM_018979.3(WNK1):c.5290G>T (p.Val1764Leu) rs201521760
NM_018979.3(WNK1):c.5314A>C (p.Thr1772Pro)
NM_018979.3(WNK1):c.5492C>G (p.Thr1831Arg) rs373765496
NM_018979.3(WNK1):c.5496G>T (p.Gln1832His)
NM_018979.3(WNK1):c.5525_5527delAAG (p.Glu1842del)
NM_018979.3(WNK1):c.5530C>T (p.Pro1844Ser) rs769345308
NM_018979.3(WNK1):c.564C>T (p.Gly188=) rs72647371
NM_018979.3(WNK1):c.5720C>T (p.Pro1907Leu) rs200979623
NM_018979.3(WNK1):c.5768A>T (p.Glu1923Val)
NM_018979.3(WNK1):c.578C>A (p.Pro193Gln) rs72647372
NM_018979.3(WNK1):c.5849C>T (p.Thr1950Ile) rs1555157875
NM_018979.3(WNK1):c.5851A>G (p.Thr1951Ala)
NM_018979.3(WNK1):c.5869C>T (p.Arg1957Cys) rs201766777
NM_018979.3(WNK1):c.5943T>G (p.Phe1981Leu) rs72650765
NM_018979.3(WNK1):c.595C>G (p.Gln199Glu) rs1404174344
NM_018979.3(WNK1):c.6059G>A (p.Ser2020Asn) rs1555158125
NM_018979.3(WNK1):c.6062G>A (p.Arg2021Lys)
NM_018979.3(WNK1):c.6152G>T (p.Ser2051Ile) rs561238194
NM_018979.3(WNK1):c.6374G>A (p.Arg2125Gln) rs757825668
NM_018979.3(WNK1):c.6503A>T (p.His2168Leu) rs1555160733
NM_018979.3(WNK1):c.65C>T (p.Ala22Val) rs1245390063
NM_018979.3(WNK1):c.6624C>G (p.Ser2208Arg)
NM_018979.3(WNK1):c.6797G>T (p.Gly2266Val)
NM_018979.3(WNK1):c.7000G>A (p.Gly2334Ser) rs770326362
NM_018979.3(WNK1):c.7003G>A (p.Ala2335Thr) rs375901694
NM_018979.3(WNK1):c.7008A>G (p.Gln2336=)
NM_018979.3(WNK1):c.7021G>A (p.Gly2341Ser) rs146042595
NM_018979.3(WNK1):c.7114A>G (p.Ser2372Gly)
NM_018979.3(WNK1):c.7121C>T (p.Pro2374Leu) rs1555164537
NM_018979.3(WNK1):c.7133A>G (p.Asn2378Ser) rs1555164556
NM_018979.3(WNK1):c.7138C>T (p.Arg2380Trp) rs56262445
NM_018979.3(WNK1):c.74C>T (p.Pro25Leu) rs1211154368
NM_018979.3(WNK1):c.865T>C (p.Ser289Pro)
NM_213655.4(WNK1):c.2152C>T (p.Arg718Cys) rs786205473

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.