ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.10324-9G>A

dbSNP: rs1238809463
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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 RCV001191238 SCV001358982 likely benign Cardiomyopathy 2019-03-11 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002560107 SCV001632814 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2022-06-20 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004803548 SCV005428045 likely benign Catecholaminergic polymorphic ventricular tachycardia 2024-07-29 criteria provided, single submitter clinical testing

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