RS397507539 PTPN11
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Noonan syndrome
Noonan syndrome 1
RASopathy
Juvenile myelomonocytic leukemia
LEOPARD syndrome 1
Metachondromatosis
Cardiovascular phenotype
RASopathy
Noonan syndrome
Noonan syndrome 1
Noonan syndrome and Noonan-related syndrome
LEOPARD syndrome 1
Juvenile myelomonocytic leukemia
Metachondromatosis
Noonan syndrome 1
Other Variants in PTPN11