RS761389904 NDUFAF5

Health Risk Chr 20:13816520
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Mitochondrial complex I deficiency
nuclear type 16
Leigh syndrome
Inborn genetic diseases
Mitochondrial complex I deficiency
nuclear type 16
Leigh syndrome
Other Variants in NDUFAF5
rs118203929 rs267606689 rs139219896 rs150955045 rs576780935 rs746405080 rs531254130 rs150613320 rs755097467 rs757043077
Ask Dr. Hemsworth about this variant