RS121918477 F2

Health Risk Chr 11:46726563
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What This Variant Does
"[OMIM:?]
Associated Conditions
Congenital prothrombin deficiency
Thrombophilia due to thrombin defect
Congenital prothrombin deficiency
Thrombophilia due to thrombin defect
Other Variants in F2
rs62623459 rs121918478 rs121918479 rs121918480 rs121918481 rs121918482 rs387906522 rs1799963 rs121918483 rs121918484
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