RS200286768 MTFMT

Health Risk Chr 15:65003238
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What This Variant Does
"CLNSIG=5
Associated Conditions
Mitochondrial complex I deficiency
nuclear type 27
Combined oxidative phosphorylation defect type 15
Inborn genetic diseases
MTFMT-Related Disorders
MTFMT-related disorder
Mitochondrial complex I deficiency
nuclear type 27
Combined oxidative phosphorylation defect type 15
Inborn genetic diseases
MTFMT-Related Disorders
MTFMT-related disorder
Other Variants in MTFMT
rs201431517 rs397514613 rs397514614 rs587777244 rs587777417 rs587777418 rs587777419 rs863224897 rs372732702 rs1064793194
Ask Dr. Hemsworth about this variant