RS867723941 NDUFS8

Health Risk Chr 11:68033218
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Associated Conditions
Mitochondrial complex I deficiency
nuclear type 2
Inborn genetic diseases
Mitochondrial complex I deficiency
nuclear type 2
Inborn genetic diseases
Other Variants in NDUFS8
rs142658611 rs199793417 rs370053943 rs144125742 rs1131691492 rs750075208 rs143337739 rs1267554976 rs2495580894 rs1267270290
Ask Dr. Hemsworth about this variant