RS1555066709 FOXRED1

Health Risk Chr 11:126277071
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Associated Conditions
Inborn genetic diseases
Leigh syndrome
Mitochondrial complex I deficiency
nuclear type 19
Inborn genetic diseases
Leigh syndrome
Mitochondrial complex I deficiency
nuclear type 19
Other Variants in FOXRED1
rs267606829 rs267606830 rs387907087 rs398124308 rs148346044 rs34542988 rs28372779 rs143739550 rs7116126 rs368307265
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