ClinVar Miner

Submissions for variant NM_001943.5(DSG2):c.1848G>C (p.Ala616=)

dbSNP: rs372349945
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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 RCV001177229 SCV001341404 likely benign Cardiomyopathy 2019-09-09 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003517306 SCV004276094 likely benign Arrhythmogenic right ventricular dysplasia 10 2024-01-04 criteria provided, single submitter clinical testing

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