RS397507483 BRAF

Health Risk Chr 7:140753348
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What This Variant Does
"aka c.1787G&gt
Associated Conditions
RASopathy
Cardio-facio-cutaneous syndrome
Noonan syndrome
Cardiofaciocutaneous syndrome 1
Inborn genetic diseases
BRAF-related disorder
RASopathy
Cardio-facio-cutaneous syndrome
Noonan syndrome
Cardiofaciocutaneous syndrome 1
Inborn genetic diseases
BRAF-related disorder
Other Variants in BRAF
rs1586126439 rs113488022 rs180177032 rs180177033 rs121913348 rs180177034 rs121913364 rs121913351 rs121913366 rs121913369
Ask Dr. Hemsworth about this variant