ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.1481+423G>A

gnomAD frequency: 0.29414  dbSNP: rs12304811
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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 RCV000942917 SCV001088854 benign Long QT syndrome 2019-12-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004707492 SCV005234668 benign not provided criteria provided, single submitter not provided

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