ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.1953T>C (p.His651=)

dbSNP: rs1663595328
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV001311690 SCV001501967 likely benign not provided 2021-01-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002545042 SCV001698676 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2020-08-14 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004005057 SCV004831515 likely benign Catecholaminergic polymorphic ventricular tachycardia 2023-06-26 criteria provided, single submitter clinical testing

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