RS374997012 TWNK

Health Risk Chr 10:100989114
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What This Variant Does
"CLNSIG=4
Associated Conditions
Infantile onset spinocerebellar ataxia
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 3
Infantile onset spinocerebellar ataxia
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 3
Other Variants in TWNK
rs2493633263 rs111033572 rs111033573 rs111033574 rs111033575 rs111033576 rs111033577 rs28937887 rs111033579 rs80356543
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