ClinVar Miner

Submissions for variant NM_032387.5(WNK4):c.1693C>G (p.Gln565Glu) (rs137853092)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000008099 SCV000028304 pathogenic Pseudohypoaldosteronism type 2B 2004-08-01 no assertion criteria provided literature only
GeneReviews RCV000008099 SCV000503029 pathogenic Pseudohypoaldosteronism type 2B 2017-02-16 no assertion criteria provided literature only

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