RS531254130 NDUFAF5

Health Risk Chr 20:13785223
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Mitochondrial complex I deficiency
nuclear type 16
Inborn genetic diseases
Mitochondrial complex I deficiency
nuclear type 16
Other Variants in NDUFAF5
rs118203929 rs267606689 rs139219896 rs150955045 rs576780935 rs746405080 rs761389904 rs150613320 rs755097467 rs757043077
Ask Dr. Hemsworth about this variant