ClinVar Miner

Submissions for variant NM_001943.5(DSG2):c.912T>C (p.Asp304=)

dbSNP: rs2510912912
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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 RCV003533632 SCV004363176 likely benign Cardiomyopathy 2022-03-09 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004011612 SCV004819494 likely benign Arrhythmogenic right ventricular cardiomyopathy 2023-11-20 criteria provided, single submitter clinical testing

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