Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Equipe Genetique des Anomalies du Developpement, |
RCV000824993 | SCV000966178 | pathogenic | Noonan syndrome 7 | 2018-07-24 | criteria provided, single submitter | clinical testing |