ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.9943T>C (p.Leu3315=)

dbSNP: rs2149066640
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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 RCV002557535 SCV001655559 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2020-09-15 criteria provided, single submitter clinical testing

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