RS397507469 BRAF

Health Risk Chr 7:140801503
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What This Variant Does
"CLNSIG=5
Associated Conditions
Noonan syndrome
Cardio-facio-cutaneous syndrome
Inborn genetic diseases
RASopathy
Noonan syndrome
Cardio-facio-cutaneous syndrome
Inborn genetic diseases
RASopathy
Other Variants in BRAF
rs1586126439 rs113488022 rs180177032 rs180177033 rs121913348 rs180177034 rs121913364 rs121913351 rs121913366 rs121913369
Ask Dr. Hemsworth about this variant