ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.14434-5dup

dbSNP: rs1662145037
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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 RCV001181660 SCV001346853 likely benign Cardiomyopathy 2018-11-16 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004803482 SCV005428179 likely benign Catecholaminergic polymorphic ventricular tachycardia 2024-08-13 criteria provided, single submitter clinical testing

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