RS11542130 TWNK

Health Risk Chr 10:100988849
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Associated Conditions
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 3
Sensory ataxic neuropathy
dysarthria
and ophthalmoparesis
Infantile onset spinocerebellar ataxia
Autosomal recessive cerebellar ataxia
Hereditary spastic paraplegia
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 3
Sensory ataxic neuropathy
dysarthria
and ophthalmoparesis
Infantile onset spinocerebellar ataxia
Autosomal recessive cerebellar ataxia
Other Variants in TWNK
rs2493633263 rs111033572 rs111033573 rs111033574 rs111033575 rs111033576 rs111033577 rs28937887 rs111033579 rs80356543
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