ClinVar Miner

Submissions for variant NM_000722.4(CACNA2D1):c.31C>T (p.Leu11=)

dbSNP: rs1830666860
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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 RCV002098073 SCV002387792 likely benign Brugada syndrome 2021-10-07 criteria provided, single submitter clinical testing

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