ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.1650A>G (p.Gln550=)

dbSNP: rs1660402221
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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 RCV001190824 SCV001358413 likely benign Cardiomyopathy 2019-10-01 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004010462 SCV004846229 likely benign Catecholaminergic polymorphic ventricular tachycardia 2023-02-24 criteria provided, single submitter clinical testing

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