RS769827124 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 recessive 1
Sensory ataxic neuropathy
dysarthria
and ophthalmoparesis
Neonatal seizure
Mitochondrial DNA depletion syndrome 4b
autosomal dominant 1
POLG-related disorder
Progressive sclerosing poliodystrophy
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal recessive 1
Sensory ataxic neuropathy
dysarthria
Other Variants in POLG