Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genome Diagnostics Laboratory, |
RCV001813586 | SCV002060823 | uncertain significance | Noonan syndrome and Noonan-related syndrome | 2021-03-16 | criteria provided, single submitter | clinical testing | |
Service de Génétique Moléculaire, |
RCV001261102 | SCV001438506 | uncertain significance | Noonan syndrome | no assertion criteria provided | clinical testing |