RS765775292 NDUFA10

Health Risk Chr 2:240022181
Upload your DNA to see your genotype for this variant.
Associated Conditions
Inborn genetic diseases
Mitochondrial complex I deficiency
nuclear type 22
Inborn genetic diseases
Mitochondrial complex I deficiency
nuclear type 22
Other Variants in NDUFA10
rs387906872 rs387906873 rs147876332 rs199648872 rs761149153 rs140776586 rs863224083 rs374970309 rs149783296 rs116254382
Ask Dr. Hemsworth about this variant