RS61995958 COQ8A
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive ataxia due to ubiquinone deficiency
Autosomal recessive ataxia due to ubiquinone deficiency
Autosomal recessive ataxia due to ubiquinone deficiency
Autosomal recessive ataxia due to ubiquinone deficiency
Other Variants in COQ8A