RS150613320 NDUFAF5

Health Risk Chr 20:13788652
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=255
Associated Conditions
Inborn genetic diseases
Mitochondrial complex I deficiency
nuclear type 16
nuclear type 1
NDUFAF5-related disorder
Leigh syndrome
Sarcoma
Uterine carcinosarcoma
Inborn genetic diseases
Mitochondrial complex I deficiency
nuclear type 16
nuclear type 1
NDUFAF5-related disorder
Leigh syndrome
Sarcoma
Other Variants in NDUFAF5
rs118203929 rs267606689 rs139219896 rs150955045 rs576780935 rs746405080 rs531254130 rs761389904 rs755097467 rs757043077
Ask Dr. Hemsworth about this variant