RS121918454 PTPN11
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What This Variant Does
"[OMIM:?]
Associated Conditions
Noonan syndrome 1
Noonan syndrome
Juvenile myelomonocytic leukemia
LEOPARD syndrome 1
Metachondromatosis
RASopathy
Noonan syndrome and Noonan-related syndrome
Cardiovascular phenotype
RASopathy
Pilocytic astrocytoma
Diffuse pediatric-type high-grade glioma
H3-wildtype and IDH-wildtype
Diffuse midline glioma
H3 K27M-mutant
Embryonal rhabdomyosarcoma
Other Variants in PTPN11