RS201088736 NDUFAF6

Health Risk Chr 8:95045599
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What This Variant Does
"CLNSIG=5
Associated Conditions
Mitochondrial complex I deficiency
nuclear type 17
See cases
Inborn genetic diseases
Mitochondrial complex I deficiency
nuclear type 17
See cases
Inborn genetic diseases
Other Variants in NDUFAF6
rs137853184 rs202047755 rs863223932 rs863223931 rs201732170 rs1554669910 rs768273248 rs1057519084 rs1057519085 rs758181982
Ask Dr. Hemsworth about this variant