Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Equipe Genetique des Anomalies du Developpement, |
RCV000590923 | SCV000700149 | pathogenic | X-linked intellectual disability, Cantagrel type | 2017-02-22 | criteria provided, single submitter | clinical testing |