ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.2907-4G>A

dbSNP: rs2148089177
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001805438 SCV002052698 likely benign Cardiomyopathy 2021-03-02 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004009133 SCV004818163 likely benign Catecholaminergic polymorphic ventricular tachycardia 2023-03-23 criteria provided, single submitter clinical testing

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