ClinVar Miner

Submissions for variant NM_201596.3(CACNB2):c.1389C>A (p.Ala463=)

dbSNP: rs1554842250
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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 RCV000646217 SCV000767976 likely benign Brugada syndrome 4 2017-10-24 criteria provided, single submitter clinical testing

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