RS875989827 COA6
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Cardioencephalomyopathy
fatal infantile
due to cytochrome c oxidase deficiency 4
Cardioencephalomyopathy
fatal infantile
due to cytochrome c oxidase deficiency 4
Other Variants in COA6