Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Génétique des Maladies du Développement, |
RCV000760282 | SCV000890122 | likely pathogenic | Intellectual disability, autosomal dominant 27 | 2017-12-28 | criteria provided, single submitter | clinical testing |