ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.1113+7A>G

gnomAD frequency: 0.00013  dbSNP: rs369423529
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001515449 SCV001723530 benign Long QT syndrome 2018-03-22 criteria provided, single submitter clinical testing

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