ClinVar Miner

Submissions for variant NM_001943.5(DSG2):c.1515A>T (p.Thr505=)

dbSNP: rs2073230182
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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 RCV001186103 SCV001352447 likely benign Cardiomyopathy 2018-12-16 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004008580 SCV004819553 likely benign Arrhythmogenic right ventricular cardiomyopathy 2023-12-18 criteria provided, single submitter clinical testing

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