Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Equipe Genetique des Anomalies du Developpement, |
RCV002286878 | SCV002576805 | pathogenic | Intellectual disability, autosomal dominant 20 | criteria provided, single submitter | clinical testing |