ClinVar Miner

Submissions for variant NM_001943.5(DSG2):c.696C>T (p.His232=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002880729 SCV003232820 likely benign Arrhythmogenic right ventricular dysplasia 10 2022-08-22 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004007646 SCV004837006 likely benign Arrhythmogenic right ventricular cardiomyopathy 2023-10-06 criteria provided, single submitter clinical testing

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