Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Génétique des Maladies du Développement, |
RCV001175149 | SCV001335329 | likely pathogenic | Intellectual disability, autosomal dominant 8 | criteria provided, single submitter | clinical testing |