ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.13098A>G (p.Leu4366=)

dbSNP: rs2149356435
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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 RCV002563281 SCV001697117 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2024-05-17 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004804200 SCV005428125 likely benign Catecholaminergic polymorphic ventricular tachycardia 2024-08-13 criteria provided, single submitter clinical testing

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