Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001222471 | SCV001394570 | likely benign | RASopathy | 2022-11-15 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002491699 | SCV002794272 | uncertain significance | Noonan syndrome 1; Juvenile myelomonocytic leukemia; Metachondromatosis; LEOPARD syndrome 1 | 2021-11-04 | criteria provided, single submitter | clinical testing |