RS200798080 TWNK

Health Risk Chr 10:100989311
Upload your DNA to see your genotype for this variant.
Associated Conditions
Autosomal recessive cerebellar ataxia
Infantile onset spinocerebellar ataxia
Sensory ataxic neuropathy
dysarthria
and ophthalmoparesis
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 3
Hereditary spastic paraplegia
Autosomal recessive cerebellar ataxia
Infantile onset spinocerebellar ataxia
Sensory ataxic neuropathy
dysarthria
and ophthalmoparesis
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 3
Other Variants in TWNK
rs2493633263 rs111033572 rs111033573 rs111033574 rs111033575 rs111033576 rs111033577 rs28937887 rs111033579 rs80356543
Ask Dr. Hemsworth about this variant