ClinVar Miner

Submissions for variant NM_001943.5(DSG2):c.169del (p.Ala57fs)

dbSNP: rs2510910367
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, Clinical Exome/Genome Diagnostics Group, University Hospital Bonn RCV003486406 SCV004239249 likely pathogenic Arrhythmogenic right ventricular dysplasia 10 2024-01-16 criteria provided, single submitter clinical testing

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