ClinVar Miner

Submissions for variant NM_001943.5(DSG2):c.1689del (p.Arg565fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003517518 SCV004244989 pathogenic Arrhythmogenic right ventricular dysplasia 10 2023-11-03 criteria provided, single submitter clinical testing This sequence change creates a premature translational stop signal (p.Arg565Glufs*7) in the DSG2 gene. It is expected to result in an absent or disrupted protein product. Loss-of-function variants in DSG2 are known to be pathogenic (PMID: 17105751, 31386562). This variant is not present in population databases (gnomAD no frequency). This variant has not been reported in the literature in individuals affected with DSG2-related conditions. For these reasons, this variant has been classified as Pathogenic.

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