RS397507541 PTPN11
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What This Variant Does
"CLNSIG=5
Associated Conditions
RASopathy
LEOPARD syndrome 1
Noonan syndrome 1
Noonan syndrome with multiple lentigines
Noonan syndrome
Noonan syndrome and Noonan-related syndrome
Juvenile myelomonocytic leukemia
Metachondromatosis
PTPN11-related disorder
Cardiovascular phenotype
Diffuse midline glioma
H3 K27M-mutant
RASopathy
LEOPARD syndrome 1
Noonan syndrome 1
Other Variants in PTPN11