ClinVar Miner

Submissions for variant NM_201596.3(CACNB2):c.822G>C (p.Pro274=)

dbSNP: rs199908591
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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 RCV000934117 SCV001079834 likely benign Brugada syndrome 4 2020-05-05 criteria provided, single submitter clinical testing

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