RS397507511 PTPN11

Health Risk Chr 12:112450385
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What This Variant Does
"CLNSIG=5
Associated Conditions
RASopathy
Noonan syndrome
Cardiovascular phenotype
Noonan syndrome 1
Noonan syndrome 1
Cardiovascular phenotype
Neuroblastoma
Juvenile myelomonocytic leukemia
Pilocytic astrocytoma
Diffuse midline glioma
H3 K27M-mutant
Neoplasm
RASopathy
Noonan syndrome
Cardiovascular phenotype
Other Variants in PTPN11
rs121918453 rs121918454 rs28933386 rs121918455 rs121918456 rs121918460 rs121918461 rs121918457 rs121918458 rs121918459
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