ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.12447T>C (p.Tyr4149=)

dbSNP: rs2149353878
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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 RCV002554379 SCV002341248 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2025-01-01 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004011210 SCV004826186 likely benign Catecholaminergic polymorphic ventricular tachycardia 2023-06-26 criteria provided, single submitter clinical testing

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