ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.12966T>A (p.Ala4322=)

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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 RCV003852601 SCV004661968 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2023-03-07 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004006138 SCV004819899 likely benign Catecholaminergic polymorphic ventricular tachycardia 2023-04-03 criteria provided, single submitter clinical testing

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