ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.1482-264C>T

gnomAD frequency: 0.00134  dbSNP: rs144865478
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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 RCV000860692 SCV001000820 benign Long QT syndrome 2019-12-31 criteria provided, single submitter clinical testing

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