RS1309343892 MECOM

Health Risk Chr 3:169116038
Upload your DNA to see your genotype for this variant.
Associated Conditions
Inborn genetic diseases
Radioulnar synostosis with amegakaryocytic thrombocytopenia 2
Inborn genetic diseases
Radioulnar synostosis with amegakaryocytic thrombocytopenia 2
Other Variants in MECOM
rs864309722 rs864309723 rs864309724 rs1560118923 rs148539966 rs200965422 rs572906212 rs1577005203 rs767306816 rs745797691
Ask Dr. Hemsworth about this variant