ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.705G>A (p.Arg235=)

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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 RCV003078575 SCV003474860 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2022-04-07 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004009395 SCV004826786 likely benign Catecholaminergic polymorphic ventricular tachycardia 2023-08-08 criteria provided, single submitter clinical testing

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