ClinVar Miner

Submissions for variant NM_001126108.2(SLC12A3):c.2634-9G>A

dbSNP: rs1596944843
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000981050 SCV001129014 likely benign not provided 2023-08-04 criteria provided, single submitter clinical testing
Natera, Inc. RCV001276418 SCV001462684 uncertain significance Familial hypokalemia-hypomagnesemia 2020-03-10 no assertion criteria provided clinical testing

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