ClinVar Miner

Submissions for variant NM_000722.4(CACNA2D1):c.1884C>T (p.Gly628=)

gnomAD frequency: 0.00001  dbSNP: rs752092062
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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 RCV001229540 SCV001401987 likely benign Brugada syndrome 2024-02-17 criteria provided, single submitter clinical testing

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