ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.50-162C>G

gnomAD frequency: 0.61134  dbSNP: rs2299661
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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 RCV000860298 SCV001000294 benign Long QT syndrome 2019-12-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004707411 SCV005234213 benign not provided criteria provided, single submitter not provided

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