RS397507527 PTPN11
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Noonan syndrome
RASopathy
Noonan syndrome 1
LEOPARD syndrome 1
Metachondromatosis
Noonan syndrome with multiple lentigines
PTPN11-related disorder
Cardiovascular phenotype
Monogenic short statue
Noonan syndrome
RASopathy
LEOPARD syndrome 1
Noonan syndrome 1
Juvenile myelomonocytic leukemia
Metachondromatosis
Other Variants in PTPN11