Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV002031073 | SCV002316960 | likely benign | Neurofibromatosis, type 1 | 2023-12-06 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002486764 | SCV002786485 | uncertain significance | Neurofibromatosis, familial spinal; Juvenile myelomonocytic leukemia; Neurofibromatosis, type 1; Neurofibromatosis-Noonan syndrome; Café-au-lait macules with pulmonary stenosis | 2022-03-05 | criteria provided, single submitter | clinical testing |