ClinVar Miner

Submissions for variant NM_201596.3(CACNB2):c.1302+12_1302+16dup

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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 RCV003622334 SCV004553019 likely benign Brugada syndrome 4 2023-05-31 criteria provided, single submitter clinical testing

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