ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.13575T>C (p.Ser4525=)

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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 RCV003533488 SCV004361553 likely benign Cardiomyopathy 2023-05-17 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003638975 SCV004512710 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2022-11-03 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004011562 SCV004831712 likely benign Catecholaminergic polymorphic ventricular tachycardia 2023-07-10 criteria provided, single submitter clinical testing

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