ClinVar Miner

List of variants in gene WNK1 reported as benign by Athena Diagnostics Inc

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
Download table as spreadsheet
HGVS dbSNP
NM_018979.4(WNK1):c.1287A>G (p.Ala429=) rs10774466
NM_018979.4(WNK1):c.1479T>C (p.Asp493=) rs2286006
NM_018979.4(WNK1):c.1994C>T (p.Thr665Ile) rs2286007
NM_018979.4(WNK1):c.2328G>A (p.Gln776=) rs1012729
NM_018979.4(WNK1):c.258T>C (p.Cys86=) rs3168640
NM_018979.4(WNK1):c.3166A>C (p.Thr1056Pro) rs956868
NM_018979.4(WNK1):c.3489+4C>T rs34032084
NM_018979.4(WNK1):c.3960C>T (p.Asn1320=) rs7300444
NM_018979.4(WNK1):c.4044C>T (p.Thr1348=) rs10849577
NM_018979.4(WNK1):c.421G>A (p.Ala141Thr) rs11554421
NM_018979.4(WNK1):c.4517G>C (p.Cys1506Ser) rs7955371
NM_018979.4(WNK1):c.5424G>T (p.Met1808Ile) rs12828016
NM_018979.4(WNK1):c.5468C>T (p.Pro1823Leu) rs17755373
NM_018979.4(WNK1):c.6828C>T (p.Tyr2276=) rs4766334
NM_018979.4(WNK1):c.759+15A>C rs11064518
NM_018979.4(WNK1):c.759+18_759+19dup rs1565378497

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.