RS28939711 COX15

Health Risk Chr 10:99724057
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What This Variant Does
"[OMIM:CARDIOMYOPATHY, HYPERTROPHIC, EARLY-ONSET FATAL]
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
Inborn genetic diseases
Other Variants in COX15
rs397514662 rs2231678 rs542092025 rs141830307 rs138293000 rs777532861 rs151116399 rs141066870 rs200910834 rs79410539
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