RS376607329 PTPN11

Health Risk Chr 12:112472981
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What This Variant Does
"c.794G&gt
Associated Conditions
Noonan syndrome
Noonan syndrome 1
RASopathy
PTPN11-related disorder
Metachondromatosis
LEOPARD syndrome 1
Juvenile myelomonocytic leukemia
Cardiovascular phenotype
Monogenic short statue
Cardiovascular phenotype
RASopathy
PTPN11-related disorder
Noonan syndrome
Noonan syndrome 1
RASopathy
Other Variants in PTPN11
rs121918453 rs121918454 rs28933386 rs121918455 rs121918456 rs121918460 rs121918461 rs121918457 rs121918458 rs121918459
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