RS387907087 FOXRED1

Health Risk Chr 11:126276476
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Mitochondrial complex I deficiency
nuclear type 19
Inborn genetic diseases
Mitochondrial complex I deficiency
nuclear type 19
Inborn genetic diseases
Other Variants in FOXRED1
rs267606829 rs267606830 rs398124308 rs148346044 rs34542988 rs28372779 rs143739550 rs7116126 rs368307265 rs372318280
Ask Dr. Hemsworth about this variant