RS948273916 F2

Health Risk Chr 11:46725928
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Associated Conditions
Inborn genetic diseases
Congenital prothrombin deficiency
Inborn genetic diseases
Congenital prothrombin deficiency
Other Variants in F2
rs62623459 rs121918477 rs121918478 rs121918479 rs121918480 rs121918481 rs121918482 rs387906522 rs1799963 rs121918483
Ask Dr. Hemsworth about this variant