RS148234280 TWNK
Upload your DNA to see your genotype for this variant.
Associated Conditions
Infantile onset spinocerebellar ataxia
Sensory ataxic neuropathy
dysarthria
and ophthalmoparesis
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 3
Autosomal recessive cerebellar ataxia
Hereditary spastic paraplegia
Infantile onset spinocerebellar ataxia
Sensory ataxic neuropathy
dysarthria
and ophthalmoparesis
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 3
Autosomal recessive cerebellar ataxia
Other Variants in TWNK