RS137852863 NDUFAF2

Health Risk Chr 5:61073136
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What This Variant Does
"[OMIM:?]
Associated Conditions
Mitochondrial complex I deficiency
nuclear type 10
nuclear type 1
Inborn genetic diseases
Leigh syndrome
Mitochondrial complex I deficiency
nuclear type 10
nuclear type 1
Inborn genetic diseases
Leigh syndrome
Other Variants in NDUFAF2
rs2531892073 rs1554076309 rs550008432 rs1752321639 rs1561557254 rs761787794 rs376747316 rs1750415294 rs2531892396 rs2532030623
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