ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.11505C>T (p.Phe3835=)

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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 RCV002889529 SCV003232319 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2023-10-10 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004007648 SCV004842527 likely benign Catecholaminergic polymorphic ventricular tachycardia 2023-12-13 criteria provided, single submitter clinical testing

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