RS571011689 MFN2
Upload your DNA to see your genotype for this variant.
Associated Conditions
Charcot-Marie-Tooth disease type 2
Hereditary motor and sensory neuropathy with optic atrophy
Inborn genetic diseases
MFN2-related disorder
Charcot-Marie-Tooth disease type 2
Hereditary motor and sensory neuropathy with optic atrophy
Inborn genetic diseases
MFN2-related disorder
Other Variants in MFN2