ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.2103+12T>C

dbSNP: rs2153223930
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001718044 SCV001945156 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005094898 SCV005771528 likely benign Long QT syndrome 2024-02-06 criteria provided, single submitter clinical testing

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