ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.916+15C>T

gnomAD frequency: 0.00033  dbSNP: rs201265381
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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 RCV002124924 SCV002405712 benign Long QT syndrome 2023-11-10 criteria provided, single submitter clinical testing

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