RS397515440 NUBPL

Health Risk Chr 14:31599310
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What This Variant Does
"CLNSIG=5
Associated Conditions
Mitochondrial complex I deficiency
nuclear type 21
Inborn genetic diseases
Mitochondrial complex I deficiency
nuclear type 21
Inborn genetic diseases
Other Variants in NUBPL
rs200401432 rs879255565 rs751631278 rs552722349 rs118161496 rs45468395 rs201430951 rs34570972 rs749681373 rs377077969
Ask Dr. Hemsworth about this variant