ClinVar Miner

Submissions for variant NM_000722.4(CACNA2D1):c.355-14dup

dbSNP: rs142849270
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000200585 SCV000252728 benign Brugada syndrome 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV001722101 SCV000730186 benign not provided 2018-06-11 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV000602132 SCV001920609 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV000602132 SCV001952393 benign not specified no assertion criteria provided clinical testing

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