ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.4957-207C>T

gnomAD frequency: 0.03372  dbSNP: rs111800411
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000860506 SCV001000573 benign Long QT syndrome 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV001664486 SCV001873460 benign not provided 2018-06-26 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001664486 SCV005234722 benign not provided criteria provided, single submitter not provided

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