RS28937887 TWNK

Health Risk Chr 10:100989211
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What This Variant Does
"[OMIM:PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, DIGENIC]
Associated Conditions
Progressive external ophthalmoplegia with mitochondrial DNA deletions
digenic
Mitochondrial disease
Infantile onset spinocerebellar ataxia
autosomal dominant 3
Progressive external ophthalmoplegia with mitochondrial DNA deletions
digenic
Mitochondrial disease
Infantile onset spinocerebellar ataxia
autosomal dominant 3
Other Variants in TWNK
rs2493633263 rs111033572 rs111033573 rs111033574 rs111033575 rs111033576 rs111033577 rs111033579 rs80356543 rs80356544
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