RS121918462 PTPN11
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What This Variant Does
"[OMIM:?]
Associated Conditions
Noonan syndrome 1
RASopathy
Noonan syndrome
Juvenile myelomonocytic leukemia
LEOPARD syndrome 1
Metachondromatosis
Noonan syndrome and Noonan-related syndrome
Cardiovascular phenotype
Vascular disorder
See cases
Intellectual disability
Noonan syndrome 1
RASopathy
Noonan syndrome
Juvenile myelomonocytic leukemia
Other Variants in PTPN11