RS753416225 POLG
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Associated Conditions
Hereditary spastic paraplegia
Progressive sclerosing poliodystrophy
Mitochondrial DNA depletion syndrome
Inborn genetic diseases
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 1
autosomal recessive 1
Sensory ataxic neuropathy
dysarthria
and ophthalmoparesis
Mitochondrial DNA depletion syndrome 4b
Hereditary spastic paraplegia
Progressive sclerosing poliodystrophy
Mitochondrial DNA depletion syndrome
Inborn genetic diseases
Other Variants in POLG