RS182559752 TWNK
Upload your DNA to see your genotype for this variant.
Associated Conditions
Sensory ataxic neuropathy
dysarthria
and ophthalmoparesis
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 3
Autosomal recessive cerebellar ataxia
Infantile onset spinocerebellar ataxia
Hereditary spastic paraplegia
TWNK-related disorder
Sensory ataxic neuropathy
dysarthria
and ophthalmoparesis
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 3
Autosomal recessive cerebellar ataxia
Other Variants in TWNK