ClinVar Miner

List of variants in gene WNK1 reported as benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 38
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_018979.4(WNK1):c.6828C>T (p.Tyr2276=) rs4766334 0.98834
NM_018979.4(WNK1):c.4517G>C (p.Cys1506Ser) rs7955371 0.98791
NM_018979.4(WNK1):c.258T>C (p.Cys86=) rs3168640 0.97485
NM_018979.4(WNK1):c.3166A>C (p.Thr1056Pro) rs956868 0.84165
NM_018979.4(WNK1):c.1287A>G (p.Ala429=) rs10774466 0.71926
NM_018979.4(WNK1):c.2328G>A (p.Gln776=) rs1012729 0.69563
NM_213655.5(WNK1):c.2220dup (p.Phe741fs) rs11441897 0.55139
NM_018979.4(WNK1):c.-91T>G rs3088353 0.42310
NM_018979.4(WNK1):c.5424G>T (p.Met1808Ile) rs12828016 0.40721
NM_018979.4(WNK1):c.3960C>T (p.Asn1320=) rs7300444 0.39853
NM_018979.4(WNK1):c.2529G>A (p.Gln843=) rs9804992 0.14500
NM_018979.4(WNK1):c.1401-11C>A rs11064573 0.12417
NM_018979.4(WNK1):c.1479T>C (p.Asp493=) rs2286006 0.12413
NM_018979.4(WNK1):c.4044C>T (p.Thr1348=) rs10849577 0.12407
NM_018979.4(WNK1):c.3489+4C>T rs34032084 0.09932
NM_018979.4(WNK1):c.421G>A (p.Ala141Thr) rs11554421 0.09706
NM_018979.4(WNK1):c.759+16_759+18dup rs398088143 0.08796
NM_018979.4(WNK1):c.759+15A>C rs11064518 0.05581
NM_018979.4(WNK1):c.1994C>T (p.Thr665Ile) rs2286007 0.05498
NM_018979.4(WNK1):c.1512A>G (p.Leu504=) rs56325964 0.01671
NM_018979.4(WNK1):c.2081T>C (p.Ile694Thr) rs61736905 0.01664
NM_018979.4(WNK1):c.1526T>C (p.Ile509Thr) rs34728563 0.01649
NM_018979.4(WNK1):c.5468C>T (p.Pro1823Leu) rs17755373 0.00870
NM_018979.4(WNK1):c.2020A>G (p.Thr674Ala) rs11833299 0.00803
NM_018979.4(WNK1):c.684C>T (p.Gly228=) rs72647374 0.00748
NM_018979.4(WNK1):c.3654A>G (p.Ser1218=) rs141971833 0.00316
NM_018979.4(WNK1):c.5583+3A>G rs72650758 0.00270
NM_018979.4(WNK1):c.5281-4G>A rs72650740 0.00269
NM_018979.4(WNK1):c.2490G>A (p.Pro830=) rs79816263 0.00211
NM_018979.4(WNK1):c.3582G>A (p.Glu1194=) rs72650721 0.00173
NM_018979.4(WNK1):c.4983T>C (p.Ser1661=) rs149852592 0.00072
NM_018979.4(WNK1):c.2401A>G (p.Ile801Val) rs139449198 0.00053
NM_018979.4(WNK1):c.2664A>G (p.Val888=) rs769020140 0.00012
NM_018979.4(WNK1):c.2373+21del rs5795952
NM_018979.4(WNK1):c.2373+21dup rs5795952
NM_018979.4(WNK1):c.5542_5550del (p.Thr1848_Ser1850del) rs544395150
NM_018979.4(WNK1):c.6624C>A (p.Ser2208Arg) rs72650768
NM_213655.5(WNK1):c.2175dup (p.Ile726fs) rs35706572

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.