ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.6556-15A>G

gnomAD frequency: 0.00001  dbSNP: rs1431223272
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001184867 SCV001350953 likely benign Cardiomyopathy 2018-12-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002559072 SCV002356250 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2024-07-15 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004008492 SCV004819940 likely benign Catecholaminergic polymorphic ventricular tachycardia 2023-09-04 criteria provided, single submitter clinical testing

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