RS146742525 F2

Health Risk Chr 11:46728829
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Associated Conditions
Congenital prothrombin deficiency
Inborn genetic diseases
F2-related disorder
Thrombophilia due to thrombin defect
Congenital prothrombin deficiency
Inborn genetic diseases
F2-related disorder
Thrombophilia due to thrombin defect
Other Variants in F2
rs62623459 rs121918477 rs121918478 rs121918479 rs121918480 rs121918481 rs121918482 rs387906522 rs1799963 rs121918483
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