RS11558436 NUBPL

Health Risk Chr 14:31787859
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Associated Conditions
Mitochondrial complex I deficiency
nuclear type 1
Inborn genetic diseases
NUBPL-related disorder
nuclear type 21
Mitochondrial complex I deficiency
nuclear type 1
Inborn genetic diseases
NUBPL-related disorder
nuclear type 21
Other Variants in NUBPL
rs200401432 rs879255565 rs397515440 rs751631278 rs552722349 rs118161496 rs45468395 rs201430951 rs34570972 rs749681373
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