RS397507518 PTPN11

Health Risk Chr 12:112450508
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What This Variant Does
"CLNSIG=5
Associated Conditions
Noonan syndrome
Noonan syndrome 3
RASopathy
Noonan syndrome and Noonan-related syndrome
Noonan syndrome 1
Cardiovascular phenotype
Noonan syndrome
Noonan syndrome 3
RASopathy
Noonan syndrome and Noonan-related syndrome
Noonan syndrome 1
Cardiovascular phenotype
Other Variants in PTPN11
rs121918453 rs121918454 rs28933386 rs121918455 rs121918456 rs121918460 rs121918461 rs121918457 rs121918458 rs121918459
Ask Dr. Hemsworth about this variant