ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.11533C>T (p.Leu3845=)

dbSNP: rs1694213736
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001191505 SCV001359339 likely benign Cardiomyopathy 2020-01-10 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004010519 SCV004824074 likely benign Catecholaminergic polymorphic ventricular tachycardia 2023-08-25 criteria provided, single submitter clinical testing

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