ClinVar Miner

Submissions for variant NM_201596.3(CACNB2):c.214-18G>A

dbSNP: rs2132535749
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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 RCV002218456 SCV002365577 likely benign Brugada syndrome 4 2022-03-08 criteria provided, single submitter clinical testing

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