ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.3210-15C>T

gnomAD frequency: 0.00001  dbSNP: rs1160881733
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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 RCV002168775 SCV002422596 likely benign Long QT syndrome 2022-07-14 criteria provided, single submitter clinical testing

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