ClinVar Miner

Submissions for variant NM_032387.5(WNK4):c.1684G>A (p.Glu562Lys)

dbSNP: rs137853093
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000008100 SCV000028305 pathogenic Pseudohypoaldosteronism type 2B 2001-08-10 no assertion criteria provided literature only
GeneReviews RCV000008100 SCV000503026 not provided Pseudohypoaldosteronism type 2B no assertion provided literature only

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