ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.1236A>G (p.Glu412=)

dbSNP: rs2150166360
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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 RCV002550522 SCV002327772 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2022-11-08 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004011183 SCV004830615 likely benign Catecholaminergic polymorphic ventricular tachycardia 2023-12-01 criteria provided, single submitter clinical testing

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