RS145100473 SCO2

Health Risk Chr 22:50524071
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What This Variant Does
"CLNSIG=5
Associated Conditions
Myopia 6
Cardioencephalomyopathy
fatal infantile
due to cytochrome c oxidase deficiency 1
Mitochondrial complex IV deficiency
nuclear type 1
Inborn genetic diseases
Myopia 6
Cardioencephalomyopathy
fatal infantile
due to cytochrome c oxidase deficiency 1
Mitochondrial complex IV deficiency
nuclear type 1
Inborn genetic diseases
Other Variants in SCO2
rs74315510 rs80358232 rs28937598 rs74315511 rs74315512 rs1467767014 rs28937868 rs121908508 rs767634441 rs749838192
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