Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Service de Génétique Moléculaire, |
RCV001270408 | SCV001450694 | likely pathogenic | Intellectual disability, autosomal dominant 14 | 2020-07-24 | no assertion criteria provided | clinical testing |