ClinVar Miner

Submissions for variant NM_001943.5(DSG2):c.1880-11T>C

gnomAD frequency: 0.00001  dbSNP: rs779853197
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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 RCV002088402 SCV002388038 likely benign Arrhythmogenic right ventricular dysplasia 10 2021-03-28 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV003533111 SCV004363204 likely benign Cardiomyopathy 2021-11-22 criteria provided, single submitter clinical testing

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