RS397507540 PTPN11
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What This Variant Does
"CLNSIG=5
Associated Conditions
Noonan syndrome
RASopathy
Strabismus
Short stature
Abnormal facial shape
Noonan syndrome 1
LEOPARD syndrome 1
Juvenile myelomonocytic leukemia
Metachondromatosis
Cardiovascular phenotype
RASopathy
Noonan syndrome
Noonan syndrome 1
LEOPARD syndrome 1
Noonan syndrome and Noonan-related syndrome
Other Variants in PTPN11