RS760000110 CHM

Health Risk Chr X:85956220
Upload your DNA to see your genotype for this variant.
Associated Conditions
Inborn genetic diseases
Inborn genetic diseases
Other Variants in CHM
rs132630263 rs132630264 rs132630265 rs587776746 rs132630267 rs132630266 rs397514603 rs386833676 rs527236048 rs786204761
Ask Dr. Hemsworth about this variant