RS786205570 FRAS1

Health Risk Chr 4:78478063
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in FRAS1
rs120074156 rs120074157 rs120074158 rs120074159 rs730882178 rs730882179 rs730882180 rs876661304 rs773457837 rs374045395
Ask Dr. Hemsworth about this variant