RS398124308 FOXRED1

Health Risk Chr 11:126275000
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What This Variant Does
"CLNSIG=5
Associated Conditions
Mitochondrial complex I deficiency
Leigh syndrome
nuclear type 1
nuclear type 19
Inborn genetic diseases
Mitochondrial disease
Mitochondrial complex I deficiency
Leigh syndrome
nuclear type 1
nuclear type 19
Inborn genetic diseases
Mitochondrial disease
Other Variants in FOXRED1
rs267606829 rs267606830 rs387907087 rs148346044 rs34542988 rs28372779 rs143739550 rs7116126 rs368307265 rs372318280
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