ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.6023-7A>G

gnomAD frequency: 0.00001  dbSNP: rs771502164
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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 RCV001192285 SCV001360314 likely benign Cardiomyopathy 2019-09-09 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002559210 SCV001674771 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2024-10-16 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004010592 SCV004837003 likely benign Catecholaminergic polymorphic ventricular tachycardia 2023-10-06 criteria provided, single submitter clinical testing

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