RS397507543 PTPN11

Health Risk Chr 12:112489078
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What This Variant Does
"CLNSIG=5
Associated Conditions
Noonan syndrome
RASopathy
7 conditions
Noonan syndrome 1
Cardiovascular phenotype
LEOPARD syndrome 1
Juvenile myelomonocytic leukemia
Metachondromatosis
Monogenic short statue
Noonan syndrome
RASopathy
7 conditions
Noonan syndrome 1
Cardiovascular phenotype
LEOPARD syndrome 1
Other Variants in PTPN11
rs121918453 rs121918454 rs28933386 rs121918455 rs121918456 rs121918460 rs121918461 rs121918457 rs121918458 rs121918459
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