RS746835381 NDUFAF3

Health Risk Chr 3:49023106
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Mitochondrial complex I deficiency
nuclear type 18
Inborn genetic diseases
Mitochondrial complex I deficiency
nuclear type 18
Other Variants in NDUFAF3
rs373060774 rs1064794835 rs202104160 rs138275059 rs200789117 rs199504381 rs2106770574 rs762398743 rs1242685917 rs756339822
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