RS1553877912 OPA1
Upload your DNA to see your genotype for this variant.
Associated Conditions
Abortive cerebellar ataxia
Mitochondrial DNA depletion syndrome 14 (cardioencephalomyopathic type)
Optic atrophy with or without deafness
ophthalmoplegia
myopathy
ataxia
and neuropathy
Autosomal dominant optic atrophy classic form
Abortive cerebellar ataxia
Mitochondrial DNA depletion syndrome 14 (cardioencephalomyopathic type)
Optic atrophy with or without deafness
ophthalmoplegia
myopathy
ataxia
and neuropathy
Other Variants in OPA1