RS397507529 PTPN11
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What This Variant Does
"CLNSIG=5
Associated Conditions
RASopathy
Noonan syndrome with multiple lentigines
Noonan syndrome
Noonan syndrome 1
Neurodevelopmental abnormality
Noonan syndrome and Noonan-related syndrome
LEOPARD syndrome 1
Juvenile myelomonocytic leukemia
Metachondromatosis
Cardiovascular phenotype
PTPN11-related disorder
Cleft lip/palate
RASopathy
Noonan syndrome with multiple lentigines
Noonan syndrome
Other Variants in PTPN11