RS559485096 NDUFV2

Health Risk Chr 18:9102760
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Associated Conditions
Mitochondrial complex I deficiency
nuclear type 1
nuclear type 7
Inborn genetic diseases
Mitochondrial complex I deficiency
nuclear type 1
nuclear type 7
Inborn genetic diseases
Other Variants in NDUFV2
rs538112556 rs750082630 rs2510155571 rs2510151392 rs2510155602 rs1431507497 rs756653973 rs1428682980 rs2144742205 rs754873418
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