RS111033573 TWNK

Health Risk Chr 10:100989285
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 3
Mitochondrial disease
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 3
Mitochondrial disease
Other Variants in TWNK
rs2493633263 rs111033572 rs111033574 rs111033575 rs111033576 rs111033577 rs28937887 rs111033579 rs80356543 rs80356544
Ask Dr. Hemsworth about this variant