ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.9522T>A (p.His3174Gln)

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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 RCV002595481 SCV003494003 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2024-04-15 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004009453 SCV004836126 uncertain significance Catecholaminergic polymorphic ventricular tachycardia 2024-01-05 criteria provided, single submitter clinical testing

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