ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.12408C>T (p.Ile4136=)

dbSNP: rs1294331175
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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 RCV002555159 SCV001632685 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2022-07-11 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004006977 SCV004818567 likely benign Catecholaminergic polymorphic ventricular tachycardia 2023-02-24 criteria provided, single submitter clinical testing

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