ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.3402C>T (p.Ala1134=)

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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 RCV004009778 SCV004824165 likely benign Catecholaminergic polymorphic ventricular tachycardia 2023-03-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005103208 SCV005787142 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2024-12-23 criteria provided, single submitter clinical testing

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