ClinVar Miner

Submissions for variant NM_001126108.2(SLC12A3):c.2521+278C>T

gnomAD frequency: 0.12416  dbSNP: rs16963395
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001674847 SCV001890699 benign not provided 2019-09-29 criteria provided, single submitter clinical testing
Natera, Inc. RCV001827576 SCV002089374 benign Familial hypokalemia-hypomagnesemia 2019-08-30 no assertion criteria provided clinical testing

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