RS397507501 PTPN11
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Noonan syndrome
RASopathy
Noonan syndrome 1
Noonan syndrome and Noonan-related syndrome
LEOPARD syndrome 1
Juvenile myelomonocytic leukemia
Metachondromatosis
Cardiovascular phenotype
PTPN11-related disorder
Diffuse midline glioma
H3 K27M-mutant
Noonan syndrome
RASopathy
Noonan syndrome 1
Noonan syndrome and Noonan-related syndrome
Other Variants in PTPN11