ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.5920C>T (p.Leu1974Phe)

gnomAD frequency: 0.00002  dbSNP: rs767660098
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001325995 SCV001517007 benign Long QT syndrome 2023-07-07 criteria provided, single submitter clinical testing

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