Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Equipe Genetique des Anomalies du Developpement, |
RCV000677724 | SCV000803879 | likely pathogenic | Orofaciodigital syndrome I | 2017-11-16 | criteria provided, single submitter | clinical testing |