Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Service de Génétique Moléculaire, |
RCV001255777 | SCV001432376 | likely pathogenic | Microcephaly 5, primary, autosomal recessive | no assertion criteria provided | clinical testing |