Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Equipe Genetique des Anomalies du Developpement, |
RCV000590898 | SCV000700171 | likely pathogenic | Intellectual disability, autosomal dominant 13 | 2017-01-11 | criteria provided, single submitter | clinical testing |