ClinVar Miner

Submissions for variant NM_001126108.2(SLC12A3):c.2798T>A (p.Met933Lys)

dbSNP: rs777021735
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV001277884 SCV002777826 uncertain significance Familial hypokalemia-hypomagnesemia 2022-04-01 criteria provided, single submitter clinical testing
Natera, Inc. RCV001277884 SCV001464863 uncertain significance Familial hypokalemia-hypomagnesemia 2020-08-13 no assertion criteria provided clinical testing

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