ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.10324-11_10324-10del

dbSNP: rs2149100270
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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 RCV002553037 SCV002344131 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2021-10-05 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004804355 SCV005428044 likely benign Catecholaminergic polymorphic ventricular tachycardia 2024-03-24 criteria provided, single submitter clinical testing

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