RS762093523 NDUFAF6

Health Risk Chr 8:95045546
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Associated Conditions
Inborn genetic diseases
Mitochondrial complex I deficiency
nuclear type 17
Fanconi renotubular syndrome 5
Inborn genetic diseases
Mitochondrial complex I deficiency
nuclear type 17
Fanconi renotubular syndrome 5
Other Variants in NDUFAF6
rs137853184 rs202047755 rs863223932 rs863223931 rs201732170 rs1554669910 rs201088736 rs768273248 rs1057519084 rs1057519085
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