ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.385-9A>G

dbSNP: rs140998248
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002533232 SCV000760689 benign Catecholaminergic polymorphic ventricular tachycardia 1 2024-12-19 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001184527 SCV001350521 benign Cardiomyopathy 2019-07-02 criteria provided, single submitter clinical testing

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