Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Equipe Genetique des Anomalies du Developpement, |
RCV001260510 | SCV001437531 | likely pathogenic | CEBALID syndrome | 2020-09-01 | no assertion criteria provided | clinical testing |