RS988250515 COX15
Upload your DNA to see your genotype for this variant.
Associated Conditions
Inborn genetic diseases
Cardioencephalomyopathy
fatal infantile
due to cytochrome c oxidase deficiency 2
Inborn genetic diseases
Cardioencephalomyopathy
fatal infantile
due to cytochrome c oxidase deficiency 2
Other Variants in COX15