Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Service de Génétique Moléculaire, |
RCV001580210 | SCV001809842 | pathogenic | Noonan syndrome | 2021-03-01 | no assertion criteria provided | clinical testing | |
OMIM | RCV001836619 | SCV002097231 | pathogenic | Noonan syndrome 14 | 2022-02-15 | no assertion criteria provided | literature only |