Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000552800 | SCV000659074 | likely benign | RASopathy | 2023-12-19 | criteria provided, single submitter | clinical testing | |
Genome Diagnostics Laboratory, |
RCV001813506 | SCV002060705 | uncertain significance | Noonan syndrome and Noonan-related syndrome | 2016-12-12 | criteria provided, single submitter | clinical testing |