ClinVar Miner

List of variants in gene WNK1 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
Download table as spreadsheet
HGVS dbSNP
NM_018979.4(WNK1):c.2139+2872T>C rs72649808
NM_018979.4(WNK1):c.2139+3331G>A
NM_018979.4(WNK1):c.2140-2593T>C
NM_018979.4(WNK1):c.2490G>A (p.Pro830=) rs79816263
NM_018979.4(WNK1):c.4605_4607del (p.Ser1536del) rs567183841
NM_018979.4(WNK1):c.5509+166G>A
NM_018979.4(WNK1):c.6643+136G>A

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.