ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.5680+12G>A

dbSNP: rs761437891
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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 RCV002132226 SCV002405270 benign Long QT syndrome 2024-01-29 criteria provided, single submitter clinical testing

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