ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.7431G>A (p.Gly2477=)

dbSNP: rs1347991904
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001804332 SCV002052358 likely benign Cardiomyopathy 2021-04-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002542380 SCV002456235 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2020-12-22 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004009084 SCV004814302 likely benign Catecholaminergic polymorphic ventricular tachycardia 2024-02-05 criteria provided, single submitter clinical testing

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