ClinVar Miner

Submissions for variant NM_032387.5(WNK4):c.1682C>T (p.Pro561Leu) (rs193922735)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneReviews RCV000417199 SCV000503025 pathogenic Pseudohypoaldosteronism type 2B 2017-02-16 no assertion criteria provided literature only

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