ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.7377G>C (p.Gly2459=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
All of Us Research Program, National Institutes of Health RCV004016653 SCV004836903 likely benign Catecholaminergic polymorphic ventricular tachycardia 2023-10-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005064982 SCV005694760 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2024-08-15 criteria provided, single submitter clinical testing

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