ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.5784+149G>A

gnomAD frequency: 0.02145  dbSNP: rs113077320
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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 RCV000860963 SCV001001153 benign Long QT syndrome 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV001672963 SCV001886609 benign not provided 2018-07-09 criteria provided, single submitter clinical testing

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