RS763393580 POLG
Upload your DNA to see your genotype for this variant.
Associated Conditions
Progressive sclerosing poliodystrophy
Inborn genetic diseases
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal recessive 1
Sensory ataxic neuropathy
dysarthria
and ophthalmoparesis
autosomal dominant 1
Mitochondrial DNA depletion syndrome 4b
Mitochondrial DNA depletion syndrome
POLG-related disorder
Progressive sclerosing poliodystrophy
Progressive sclerosing poliodystrophy
Inborn genetic diseases
Progressive external ophthalmoplegia with mitochondrial DNA deletions
Other Variants in POLG