RS201732356 POLG
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Progressive sclerosing poliodystrophy
6 conditions
Childhood myocerebrohepatopathy spectrum
Mitochondrial disease
Abnormality of the nervous system
Mitochondrial DNA depletion syndrome 4b
Recessive mitochondrial ataxia syndrome
Sensory ataxic neuropathy
dysarthria
and ophthalmoparesis
POLG-related disorder
Mitochondrial DNA depletion syndrome
Progressive sclerosing poliodystrophy
Mitochondrial DNA depletion syndrome
Progressive sclerosing poliodystrophy
Other Variants in POLG