RS104894632 POLG2

Health Risk Chr 17:64477929
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What This Variant Does
"[OMIM:?]
Associated Conditions
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 4
POLG2-related disorder
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 4
POLG2-related disorder
Other Variants in POLG2
rs397514659 rs1568079613 rs148941150 rs139282177 rs200118378 rs144148008 rs146504115 rs181583071 rs886037843 rs148101254
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