ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.2853+440G>A

gnomAD frequency: 0.02504  dbSNP: rs113064994
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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 RCV000861067 SCV001001280 benign Long QT syndrome 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV001538618 SCV001756295 benign not provided 2018-06-26 criteria provided, single submitter clinical testing

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