RS201430951 NUBPL

Health Risk Chr 14:31599308
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What This Variant Does
"CLNSIG=5
Associated Conditions
Mitochondrial complex I deficiency
Inborn genetic diseases
nuclear type 21
Mitochondrial complex I deficiency
Inborn genetic diseases
nuclear type 21
Other Variants in NUBPL
rs200401432 rs879255565 rs397515440 rs751631278 rs552722349 rs118161496 rs45468395 rs34570972 rs749681373 rs377077969
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