ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.3107C>G (p.Thr1036Ser)

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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 RCV002664251 SCV003524675 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2025-01-20 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004804573 SCV005426679 uncertain significance Catecholaminergic polymorphic ventricular tachycardia 2024-09-23 criteria provided, single submitter clinical testing

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