RS397507545 PTPN11
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What This Variant Does
"CLNSIG=5
Associated Conditions
RASopathy
Noonan syndrome 1
Juvenile myelomonocytic leukemia
LEOPARD syndrome 1
Metachondromatosis
Noonan syndrome
Neurodevelopmental disorder
Cardiovascular phenotype
PTPN11-related disorder
Monogenic short statue
RASopathy
Noonan syndrome
Noonan syndrome 1
Cardiovascular phenotype
LEOPARD syndrome 1
Other Variants in PTPN11