RS201431517 MTFMT

Health Risk Chr 15:65021533
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What This Variant Does
"CLNSIG=5
Associated Conditions
Combined oxidative phosphorylation defect type 15
Leigh syndrome
6 conditions
Mitochondrial complex I deficiency
nuclear type 27
See cases
Inborn genetic diseases
MTFMT-Related Disorders
MTFMT-related disorder
Combined oxidative phosphorylation defect type 15
Leigh syndrome
6 conditions
Mitochondrial complex I deficiency
nuclear type 27
See cases
Other Variants in MTFMT
rs397514613 rs397514614 rs200286768 rs587777244 rs587777417 rs587777418 rs587777419 rs863224897 rs372732702 rs1064793194
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