RS767709505 POLG
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Progressive sclerosing poliodystrophy
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 1
autosomal recessive 1
Mitochondrial DNA depletion syndrome 4b
Sensory ataxic neuropathy
dysarthria
and ophthalmoparesis
POLG-related disorder
Progressive sclerosing poliodystrophy
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 1
autosomal recessive 1
Mitochondrial DNA depletion syndrome 4b
Sensory ataxic neuropathy
Other Variants in POLG