ClinVar Miner

Submissions for variant NM_024422.6(DSC2):c.685del (p.Pro228_Leu229insTer)

dbSNP: rs1209546374
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV001771794 SCV002796035 pathogenic Arrhythmogenic right ventricular dysplasia 11 2022-01-13 criteria provided, single submitter clinical testing
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein RCV001771794 SCV002011726 pathogenic Arrhythmogenic right ventricular dysplasia 11 2021-09-28 no assertion criteria provided clinical testing

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