ClinVar Miner

Submissions for variant NM_024422.6(DSC2):c.702G>A (p.Glu234=)

dbSNP: rs397517402
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000039438 SCV000063122 likely benign not specified 2008-05-29 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001804764 SCV002052715 likely benign Cardiomyopathy 2021-04-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002054760 SCV002364556 likely benign Arrhythmogenic right ventricular dysplasia 11 2023-08-03 criteria provided, single submitter clinical testing

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