RS776887278 EPOR

Health Risk Chr 19:11381185
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Associated Conditions
Primary familial polycythemia due to EPO receptor mutation
Inborn genetic diseases
Primary familial polycythemia due to EPO receptor mutation
Inborn genetic diseases
Other Variants in EPOR
rs121918116 rs121917830 rs62638744 rs780617943 rs199645071 rs1555716523 rs370865377 rs146235694 rs1555716045 rs1555716047
Ask Dr. Hemsworth about this variant