RS1952997134 DNM1L
Upload your DNA to see your genotype for this variant.
Associated Conditions
Encephalopathy
lethal
due to defective mitochondrial peroxisomal fission 1
Inborn genetic diseases
Encephalopathy
lethal
due to defective mitochondrial peroxisomal fission 1
Inborn genetic diseases
Other Variants in DNM1L