ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.7966-11A>G

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002629966 SCV003524465 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2024-08-29 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV003533365 SCV004360676 likely benign Cardiomyopathy 2022-02-01 criteria provided, single submitter clinical testing

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