Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Equipe Genetique des Anomalies du Developpement, |
RCV000824978 | SCV000966156 | pathogenic | KBG syndrome | 2018-05-29 | criteria provided, single submitter | clinical testing |