RS147699032 F2

Health Risk Chr 11:46726142
Upload your DNA to see your genotype for this variant.
Associated Conditions
Congenital prothrombin deficiency
Inborn genetic diseases
Thrombophilia due to thrombin defect
F2-related disorder
Acute myeloid leukemia
Congenital prothrombin deficiency
Inborn genetic diseases
Thrombophilia due to thrombin defect
F2-related disorder
Acute myeloid leukemia
Other Variants in F2
rs62623459 rs121918477 rs121918478 rs121918479 rs121918480 rs121918481 rs121918482 rs387906522 rs1799963 rs121918483
Ask Dr. Hemsworth about this variant