Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Equipe Genetique des Anomalies du Developpement, |
RCV003444695 | SCV000965710 | likely pathogenic | Myoclonic-astatic epilepsy | 2015-01-01 | criteria provided, single submitter | clinical testing |