ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.11763A>G (p.Thr3921=)

dbSNP: rs1694434725
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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 RCV001179488 SCV001344158 likely benign Cardiomyopathy 2019-09-30 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004006567 SCV004824141 likely benign Catecholaminergic polymorphic ventricular tachycardia 2023-04-10 criteria provided, single submitter clinical testing

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