ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.2397-15G>A

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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 RCV003077431 SCV003461983 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2024-11-13 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV003533348 SCV004360532 likely benign Cardiomyopathy 2021-12-20 criteria provided, single submitter clinical testing

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