ClinVar Miner

Submissions for variant NM_000722.4(CACNA2D1):c.178-21dup

dbSNP: rs5885290
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001704802 SCV000730188 benign not provided 2018-06-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002064386 SCV002394346 benign Brugada syndrome 2025-02-03 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV000614151 SCV001921588 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV000614151 SCV001959652 benign not specified no assertion criteria provided clinical testing

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