RS180177042 BRAF
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Cardiofaciocutaneous syndrome 1
Inborn genetic diseases
Noonan syndrome 7
LEOPARD syndrome 3
Noonan syndrome 1
Lung carcinoma
RASopathy
Cardio-facio-cutaneous syndrome
Inborn genetic diseases
RASopathy
Cardiofaciocutaneous syndrome 1
Noonan syndrome 1
Melanoma
BRAF-related disorder
Noonan syndrome 7
Other Variants in BRAF