RS199874519 COQ8A

Health Risk Chr 1:226986458
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Autosomal recessive ataxia due to ubiquinone deficiency
Familial cancer of breast
Inborn genetic diseases
Autosomal recessive ataxia due to ubiquinone deficiency
Familial cancer of breast
Other Variants in COQ8A
rs119468004 rs119468005 rs119468006 rs387906298 rs606231138 rs606231139 rs119468008 rs387906299 rs35582308 rs137872711
Ask Dr. Hemsworth about this variant