RS34507711 MTFMT

Health Risk Chr 15:65003103
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Associated Conditions
Inborn genetic diseases
Combined oxidative phosphorylation defect type 15
Mitochondrial complex I deficiency
nuclear type 27
Inborn genetic diseases
Combined oxidative phosphorylation defect type 15
Mitochondrial complex I deficiency
nuclear type 27
Other Variants in MTFMT
rs201431517 rs397514613 rs397514614 rs200286768 rs587777244 rs587777417 rs587777418 rs587777419 rs863224897 rs372732702
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