ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.14133A>G (p.Gly4711=)

dbSNP: rs1487075001
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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 RCV003104122 SCV001677219 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2020-01-18 criteria provided, single submitter clinical testing

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