ClinVar Miner

List of variants reported as pathogenic for Pseudohypoaldosteronism type 2B

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 8
Download table as spreadsheet
NM_032387.5(WNK4):c.1679A>G (p.Glu560Gly) rs193922734
NM_032387.5(WNK4):c.1682C>T (p.Pro561Leu) rs193922735
NM_032387.5(WNK4):c.1684G>A (p.Glu562Lys) rs137853093
NM_032387.5(WNK4):c.1690G>C (p.Asp564His) rs193922736
NM_032387.5(WNK4):c.1691A>C (p.Asp564Ala) rs137853094
NM_032387.5(WNK4):c.1693C>G (p.Gln565Glu) rs137853092
NM_032387.5(WNK4):c.3505A>G (p.Lys1169Glu) rs193922737
NM_032387.5(WNK4):c.3553C>T (p.Arg1185Cys) rs137853095

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.