ClinVar Miner

Submissions for variant NM_201596.3(CACNB2):c.301C>A (p.Arg101=)

dbSNP: rs1357911128
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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 RCV002109541 SCV002398901 likely benign Brugada syndrome 4 2021-04-05 criteria provided, single submitter clinical testing

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