RS886048338 F2

Health Risk Chr 11:46729528
Upload your DNA to see your genotype for this variant.
Associated Conditions
Congenital prothrombin deficiency
Thrombophilia due to thrombin defect
Inborn genetic diseases
Thrombophilia due to thrombin defect
Congenital prothrombin deficiency
Thrombophilia due to thrombin defect
Inborn genetic diseases
Thrombophilia due to thrombin defect
Other Variants in F2
rs62623459 rs121918477 rs121918478 rs121918479 rs121918480 rs121918481 rs121918482 rs387906522 rs1799963 rs121918483
Ask Dr. Hemsworth about this variant