RS746019378 NDUFA10

Health Risk Chr 2:240014803
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Associated Conditions
Mitochondrial complex I deficiency
nuclear type 22
Leigh syndrome
Inborn genetic diseases
Mitochondrial complex I deficiency
nuclear type 22
Leigh syndrome
Inborn genetic diseases
Other Variants in NDUFA10
rs387906872 rs387906873 rs147876332 rs199648872 rs761149153 rs140776586 rs863224083 rs374970309 rs149783296 rs116254382
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