RS74315511 SCO2

Health Risk Chr 22:50523994
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What This Variant Does
"[OMIM:?]
Associated Conditions
Cardioencephalomyopathy
fatal infantile
due to cytochrome c oxidase deficiency 1
Myopia 6
Severe global developmental delay
Seizure
Tip-toe gait
SCO2-related disorder
Cardioencephalomyopathy
fatal infantile
due to cytochrome c oxidase deficiency 1
Myopia 6
Severe global developmental delay
Seizure
Tip-toe gait
Other Variants in SCO2
rs74315510 rs80358232 rs28937598 rs74315512 rs1467767014 rs28937868 rs121908508 rs145100473 rs767634441 rs749838192
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