RS9911283 TOP3A
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Associated Conditions
Microcephaly
growth restriction
and increased sister chromatid exchange 2
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal recessive 5
TOP3A-related disorder
Inborn genetic diseases
Microcephaly
growth restriction
and increased sister chromatid exchange 2
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal recessive 5
TOP3A-related disorder
Inborn genetic diseases
Other Variants in TOP3A