ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.2794-136G>T

gnomAD frequency: 0.01925  dbSNP: rs56269265
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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 RCV000860433 SCV001000487 benign Long QT syndrome 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV001577246 SCV001804594 likely benign not provided 2018-06-26 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001577246 SCV005213565 likely benign not provided criteria provided, single submitter not provided

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