RS121918453 PTPN11
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What This Variant Does
"[OMIM:?]
Associated Conditions
Noonan syndrome 1
RASopathy
Noonan syndrome
LEOPARD syndrome 1
Juvenile myelomonocytic leukemia
Metachondromatosis
Noonan syndrome and Noonan-related syndrome
Cardiovascular phenotype
Noonan syndrome
RASopathy
Noonan syndrome with multiple lentigines
Cardiovascular phenotype
RASopathy
Juvenile myelomonocytic leukemia
Noonan syndrome
Other Variants in PTPN11