ClinVar Miner

Submissions for variant NM_001943.5(DSG2):c.834A>G (p.Glu278=)

dbSNP: rs2073150921
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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 RCV001175704 SCV001339413 likely benign Cardiomyopathy 2018-10-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002558789 SCV002978517 likely benign Arrhythmogenic right ventricular dysplasia 10 2022-09-03 criteria provided, single submitter clinical testing

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