ClinVar Miner

Submissions for variant NM_024422.6(DSC2):c.1980T>C (p.Ser660=)

dbSNP: rs1986841255
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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 RCV001191175 SCV001358880 likely benign Cardiomyopathy 2019-08-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002069144 SCV002479356 likely benign Arrhythmogenic right ventricular dysplasia 11 2025-01-07 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004807447 SCV005427445 likely benign Familial isolated arrhythmogenic right ventricular dysplasia 2024-06-11 criteria provided, single submitter clinical testing

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