ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.13587A>G (p.Glu4529=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
All of Us Research Program, National Institutes of Health RCV004009801 SCV004817387 likely benign Catecholaminergic polymorphic ventricular tachycardia 2023-03-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005103210 SCV005801487 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2024-02-18 criteria provided, single submitter clinical testing

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