ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.10974T>C (p.Thr3658=)

dbSNP: rs2149168019
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002552698 SCV001599715 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2021-08-23 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001806166 SCV002052600 likely benign Cardiomyopathy 2021-04-06 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004006877 SCV004818570 likely benign Catecholaminergic polymorphic ventricular tachycardia 2023-08-15 criteria provided, single submitter clinical testing

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