ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.1740A>G (p.Val580=)

dbSNP: rs2150412954
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001779461 SCV002014876 likely benign not specified 2021-10-02 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004009050 SCV004841108 likely benign Catecholaminergic polymorphic ventricular tachycardia 2023-10-02 criteria provided, single submitter clinical testing

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