ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.8208+18T>A

dbSNP: rs1340011974
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003015282 SCV002397195 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2021-09-16 criteria provided, single submitter clinical testing

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