ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.464-8A>T

dbSNP: rs10925391
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Genetics, Academic Medical Center RCV001700541 SCV001919012 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001724403 SCV001955725 likely benign not provided no assertion criteria provided clinical testing

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