ClinVar Miner

Submissions for variant NM_024422.6(DSC2):c.1140T>C (p.Asp380=)

dbSNP: rs1252165791
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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 RCV001182883 SCV001348482 likely benign Cardiomyopathy 2019-09-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001406552 SCV001608507 likely benign Arrhythmogenic right ventricular dysplasia 11 2019-01-27 criteria provided, single submitter clinical testing

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