ClinVar Miner

Submissions for variant NM_201596.3(CACNB2):c.1182A>G (p.Val394=)

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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 RCV002676237 SCV002984198 likely benign Brugada syndrome 4 2023-09-13 criteria provided, single submitter clinical testing

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