ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.4684-5G>T

dbSNP: rs7522981
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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 RCV001180893 SCV001345945 likely benign Cardiomyopathy 2018-12-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002558976 SCV003210743 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2022-06-10 criteria provided, single submitter clinical testing

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