ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.3357-517T>C

gnomAD frequency: 0.20720  dbSNP: rs215994
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000942910 SCV001088847 benign Long QT syndrome 2019-12-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004707490 SCV005234692 benign not provided criteria provided, single submitter not provided

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