| Submitter |
RCV |
SCV |
Clinical significance |
Condition |
Last evaluated |
Review status |
Method |
Comment |
| Fulgent Genetics, Fulgent Genetics |
RCV005006806 |
SCV005632277 |
uncertain significance |
Noonan syndrome 1; Juvenile myelomonocytic leukemia; Metachondromatosis; LEOPARD syndrome 1 |
2024-06-09 |
criteria provided, single submitter |
clinical testing |
|
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