ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.773+18T>C

gnomAD frequency: 0.00001  dbSNP: rs758435186
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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 RCV003015299 SCV002400827 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2023-09-10 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003235674 SCV003934702 uncertain significance not specified 2023-05-28 criteria provided, single submitter clinical testing

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