RS121918456 PTPN11
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Noonan syndrome with multiple lentigines
RASopathy
LEOPARD syndrome 1
CBL-related disorder
Cardiovascular phenotype
Metachondromatosis
Noonan syndrome 1
Juvenile myelomonocytic leukemia
Noonan syndrome
Noonan syndrome and Noonan-related syndrome
PTPN11-related disorder
LEOPARD syndrome 1
RASopathy
Noonan syndrome 1
Noonan syndrome with multiple lentigines
Other Variants in PTPN11