RS766294940 RNASEH1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal recessive 2
Inborn genetic diseases
Possible mitochondrial disorder - nuclear genes
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal recessive 2
Inborn genetic diseases
Possible mitochondrial disorder - nuclear genes
Other Variants in RNASEH1