RS201897431 NDUFS2

Health Risk Chr 1:161213891
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Associated Conditions
Inborn genetic diseases
Mitochondrial complex I deficiency
nuclear type 6
Inborn genetic diseases
Mitochondrial complex I deficiency
nuclear type 6
Other Variants in NDUFS2
rs121434427 rs121434428 rs121434429 rs76309459 rs202121443 rs142594036 rs190184430 rs74124661 rs201554004 rs772424969
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