ClinVar Miner

Submissions for variant NM_013266.4(CTNNA3):c.844-15G>A

gnomAD frequency: 0.00098  dbSNP: rs201089736
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002070361 SCV002404899 benign Arrhythmogenic right ventricular dysplasia 13 2025-01-22 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001529381 SCV001742725 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV001699810 SCV001924245 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001699810 SCV001931603 benign not specified no assertion criteria provided clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001699810 SCV001951394 benign not specified no assertion criteria provided clinical testing

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