ClinVar Miner

Submissions for variant NM_024422.6(DSC2):c.489G>T (p.Thr163=)

dbSNP: rs752952811
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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 RCV001182819 SCV001348414 likely benign Cardiomyopathy 2018-11-30 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004008327 SCV004819342 likely benign Familial isolated arrhythmogenic right ventricular dysplasia 2023-10-27 criteria provided, single submitter clinical testing

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