RS201477273 POLG
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What This Variant Does
"CLNSIG=5
Associated Conditions
Progressive sclerosing poliodystrophy
Mitochondrial DNA depletion syndrome 4b
Spinocerebellar atrophy
Inborn genetic diseases
Hereditary spastic paraplegia
MELAS syndrome
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal recessive 1
POLG-related disorder
Mitochondrial disease
autosomal dominant 1
Sensory ataxic neuropathy
dysarthria
and ophthalmoparesis
6 conditions
Other Variants in POLG