ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.10690-4T>A

dbSNP: rs1219349222
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001179885 SCV001344685 likely benign Cardiomyopathy 2018-12-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002560796 SCV002356180 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2021-10-01 criteria provided, single submitter clinical testing

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