RS397517076 CBL
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What This Variant Does
"CLNSIG=5
Associated Conditions
Noonan syndrome
Inborn genetic diseases
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
RASopathy
CBL-related disorder
Juvenile myelomonocytic leukemia
Acute myeloid leukemia
Noonan syndrome
RASopathy
CBL-related disorder
Fragile site 11b
Glioma susceptibility 1
Cardiovascular phenotype
Noonan syndrome
Inborn genetic diseases
Other Variants in CBL