ClinVar Miner

Submissions for variant NM_201596.3(CACNB2):c.457-17T>G

dbSNP: rs4485000
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000253486 SCV000317159 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001651294 SCV001864654 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Invitae RCV000615336 SCV002446086 benign Brugada syndrome 4 2024-02-01 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV000615336 SCV000732936 benign Brugada syndrome 4 no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV000253486 SCV001919269 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV000253486 SCV001956130 benign not specified no assertion criteria provided clinical testing

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