RS148941150 POLG2
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Associated Conditions
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 4
Mitochondrial dna depletion syndrome 16B (neuroophthalmic type)
Mitochondrial DNA depletion syndrome 16 (hepatic type)
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 4
Mitochondrial dna depletion syndrome 16B (neuroophthalmic type)
Mitochondrial DNA depletion syndrome 16 (hepatic type)
Other Variants in POLG2