RS1603441682 SCO2

Health Risk Chr 22:50524410
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Associated Conditions
Cardioencephalomyopathy
fatal infantile
due to cytochrome c oxidase deficiency 1
Alagille syndrome due to a JAG1 point mutation
Cardioencephalomyopathy
fatal infantile
due to cytochrome c oxidase deficiency 1
Alagille syndrome due to a JAG1 point mutation
Other Variants in SCO2
rs74315510 rs80358232 rs28937598 rs74315511 rs74315512 rs1467767014 rs28937868 rs121908508 rs145100473 rs767634441
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