ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.3157-175C>T

gnomAD frequency: 0.00338  dbSNP: rs146526882
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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 RCV000860693 SCV001000821 benign Long QT syndrome 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV001585799 SCV001812555 likely benign not provided 2018-09-22 criteria provided, single submitter clinical testing

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