Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Equipe Genetique des Anomalies du Developpement, |
RCV000590903 | SCV000700151 | likely pathogenic | Developmental and epileptic encephalopathy, 14 | 2016-11-01 | criteria provided, single submitter | clinical testing |