ClinVar Miner

Submissions for variant NM_001943.5(DSG2):c.523+24dup

dbSNP: rs77324780
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV003487000 SCV004240512 benign Cardiomyopathy 2023-06-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003631211 SCV004378779 benign Arrhythmogenic right ventricular dysplasia 10 2024-12-31 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001700594 SCV001925145 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001700594 SCV001926893 benign not specified no assertion criteria provided clinical testing

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