RS756339822 NDUFAF3

Health Risk Chr 3:49022455
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What This Variant Does
"CLNSIG=4
Associated Conditions
Mitochondrial complex I deficiency
nuclear type 1
Inborn genetic diseases
nuclear type 18
Mitochondrial complex I deficiency
nuclear type 1
Inborn genetic diseases
nuclear type 18
Other Variants in NDUFAF3
rs373060774 rs1064794835 rs202104160 rs138275059 rs200789117 rs199504381 rs2106770574 rs762398743 rs1242685917 rs746835381
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