ClinVar Miner

Submissions for variant NM_001126108.2(SLC12A3):c.852+7_852+9del

dbSNP: rs758702370
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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 RCV000909291 SCV001054089 likely benign not provided 2024-01-24 criteria provided, single submitter clinical testing
Natera, Inc. RCV001274422 SCV001458551 uncertain significance Familial hypokalemia-hypomagnesemia 2020-01-17 no assertion criteria provided clinical testing

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