ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.3045C>T (p.Gly1015=)

dbSNP: rs1405734932
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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 RCV000774869 SCV000908888 likely benign Cardiomyopathy 2018-04-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002536691 SCV001683702 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2022-05-11 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004001418 SCV004815569 likely benign Catecholaminergic polymorphic ventricular tachycardia 2023-07-10 criteria provided, single submitter clinical testing

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