RS863223953 DNM1L

Health Risk Chr 12:32731362
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What This Variant Does
"CLNSIG=5
Associated Conditions
Encephalopathy
lethal
due to defective mitochondrial peroxisomal fission 1
Inborn genetic diseases
Optic atrophy 5
Encephalopathy
lethal
due to defective mitochondrial peroxisomal fission 1
Inborn genetic diseases
Optic atrophy 5
Other Variants in DNM1L
rs121908531 rs138620818 rs767021397 rs146565893 rs138133550 rs879253874 rs879255685 rs886037861 rs879255686 rs879255687
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