RS515726199 RRM2B
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What This Variant Does
"CLNSIG=5
Associated Conditions
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 5
RRM2B-related mitochondrial disease
Mitochondrial disease
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 5
RRM2B-related mitochondrial disease
Mitochondrial disease
Other Variants in RRM2B