RS2036859860 COX15
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Associated Conditions
Cardioencephalomyopathy
fatal infantile
due to cytochrome c oxidase deficiency 2
Inborn genetic diseases
Cardioencephalomyopathy
fatal infantile
due to cytochrome c oxidase deficiency 2
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