RS761664802 POLG

Health Risk Chr 15:89319223
Upload your DNA to see your genotype for this variant.
Associated Conditions
Progressive sclerosing poliodystrophy
Sensory ataxic neuropathy
dysarthria
and ophthalmoparesis
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 1
autosomal recessive 1
Mitochondrial DNA depletion syndrome 4b
Progressive sclerosing poliodystrophy
Sensory ataxic neuropathy
dysarthria
and ophthalmoparesis
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 1
autosomal recessive 1
Other Variants in POLG
rs113994099 rs113994095 rs121918044 rs121918045 rs121918046 rs121918048 rs121918049 rs113994098 rs113994094 rs121918047
Ask Dr. Hemsworth about this variant