ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.4140+77G>T

dbSNP: rs114714957
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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 RCV000860571 SCV001000662 benign Long QT syndrome 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV001585798 SCV001820019 likely benign not provided 2018-07-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001585798 SCV005213570 likely benign not provided criteria provided, single submitter not provided

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