RS933296601 MTFMT

Health Risk Chr 15:65029580
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Associated Conditions
Combined oxidative phosphorylation defect type 15
Inborn genetic diseases
Combined oxidative phosphorylation defect type 15
Inborn genetic diseases
Other Variants in MTFMT
rs201431517 rs397514613 rs397514614 rs200286768 rs587777244 rs587777417 rs587777418 rs587777419 rs863224897 rs372732702
Ask Dr. Hemsworth about this variant