RS112793292 SCO2
Upload your DNA to see your genotype for this variant.
Associated Conditions
Cardioencephalomyopathy
fatal infantile
due to cytochrome c oxidase deficiency 1
Myopia 6
Cardioencephalomyopathy
fatal infantile
due to cytochrome c oxidase deficiency 1
Myopia 6
Other Variants in SCO2