Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Equipe Genetique des Anomalies du Developpement, |
RCV000590947 | SCV000700164 | likely pathogenic | Developmental and epileptic encephalopathy, 24 | 2017-01-27 | criteria provided, single submitter | clinical testing |