ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.371+230A>C

gnomAD frequency: 0.01390  dbSNP: rs112435887
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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 RCV000860630 SCV001000739 benign Long QT syndrome 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV001547243 SCV001766901 likely benign not provided 2018-07-07 criteria provided, single submitter clinical testing

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