RS397507537 PTPN11

Health Risk Chr 12:112488465
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What This Variant Does
"CLNSIG=5
Associated Conditions
RASopathy
Noonan syndrome with multiple lentigines
Noonan syndrome and Noonan-related syndrome
Cardiovascular phenotype
RASopathy
Noonan syndrome with multiple lentigines
Noonan syndrome and Noonan-related syndrome
Cardiovascular phenotype
Other Variants in PTPN11
rs121918453 rs121918454 rs28933386 rs121918455 rs121918456 rs121918460 rs121918461 rs121918457 rs121918458 rs121918459
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