RS515726201 RRM2B

Health Risk Chr 8:102208223
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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
Progressive external ophthalmoplegia with mitochondrial DNA deletions
autosomal dominant 5
RRM2B-related mitochondrial disease
Other Variants in RRM2B
rs121918307 rs515726185 rs121918308 rs121918309 rs121918310 rs121918311 rs267607025 rs267607024 rs515726199 rs515726180
Ask Dr. Hemsworth about this variant