RS397507520 PTPN11

Health Risk Chr 12:112453279
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What This Variant Does
"aka c.417G&gt
Associated Conditions
RASopathy
Juvenile myelomonocytic leukemia
Noonan syndrome
Noonan syndrome 1
Inborn genetic diseases
RASopathy
Noonan syndrome 1
Noonan syndrome
LEOPARD syndrome 1
Juvenile myelomonocytic leukemia
Metachondromatosis
Cardiovascular phenotype
Noonan syndrome 3
Hypertrophic cardiomyopathy
Pectus excavatum
Other Variants in PTPN11
rs121918453 rs121918454 rs28933386 rs121918455 rs121918456 rs121918460 rs121918461 rs121918457 rs121918458 rs121918459
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