RS397507536 PTPN11
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What This Variant Does
"CLNSIG=4
Associated Conditions
Noonan syndrome 1
RASopathy
Noonan syndrome and Noonan-related syndrome
Cardiovascular phenotype
RASopathy
Noonan syndrome 1
LEOPARD syndrome 1
Metachondromatosis
Juvenile myelomonocytic leukemia
Intellectual disability
RASopathy
Noonan syndrome 1
Noonan syndrome 1
RASopathy
Noonan syndrome and Noonan-related syndrome
Other Variants in PTPN11