RS1131691575 POLG
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Associated Conditions
Mitochondrial disease
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
POLG-related disorder
Mitochondrial disease
Progressive sclerosing poliodystrophy
Inborn genetic diseases
Progressive external ophthalmoplegia with mitochondrial DNA deletions
Other Variants in POLG