RS187553791 TWNK

Health Risk Chr 10:100993929
Upload your DNA to see your genotype for this variant.
Associated Conditions
Infantile onset spinocerebellar ataxia
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 3
Sensory ataxic neuropathy
dysarthria
and ophthalmoparesis
Autosomal recessive cerebellar ataxia
Infantile onset spinocerebellar ataxia
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 3
Sensory ataxic neuropathy
dysarthria
and ophthalmoparesis
Autosomal recessive cerebellar ataxia
Other Variants in TWNK
rs2493633263 rs111033572 rs111033573 rs111033574 rs111033575 rs111033576 rs111033577 rs28937887 rs111033579 rs80356543
Ask Dr. Hemsworth about this variant