ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.4740G>T (p.Pro1580=)

dbSNP: rs79811945
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001180182 SCV001345050 likely benign Cardiomyopathy 2019-04-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002558941 SCV001693250 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2024-03-02 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004006635 SCV004823694 likely benign Catecholaminergic polymorphic ventricular tachycardia 2023-11-30 criteria provided, single submitter clinical testing

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