ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.10446C>T (p.Ala3482=)

dbSNP: rs746150182
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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 RCV001182619 SCV001348131 likely benign Cardiomyopathy 2019-01-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002559037 SCV002383102 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2022-11-12 criteria provided, single submitter clinical testing

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