RS755933881 COQ8A

Health Risk Chr 1:226982969
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Mitochondrial disease
Autosomal recessive ataxia due to ubiquinone deficiency
Inborn genetic diseases
Mitochondrial disease
Autosomal recessive ataxia due to ubiquinone deficiency
Other Variants in COQ8A
rs119468004 rs119468005 rs119468006 rs387906298 rs606231138 rs606231139 rs119468008 rs387906299 rs35582308 rs137872711
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