RS769410130 POLG
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What This Variant Does
"CLNSIG=5
Associated Conditions
Progressive sclerosing poliodystrophy
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal recessive 1
autosomal dominant 1
Inborn genetic diseases
Progressive sclerosing poliodystrophy
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal recessive 1
autosomal dominant 1
Inborn genetic diseases
Other Variants in POLG