RS5899 F2

Health Risk Chr 11:46726112
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Associated Conditions
Congenital prothrombin deficiency
Thrombophilia due to thrombin defect
F2-related disorder
Cholangiocarcinoma
Uterine corpus endometrial carcinoma
Gastric cancer
Congenital prothrombin deficiency
Thrombophilia due to thrombin defect
F2-related disorder
Cholangiocarcinoma
Uterine corpus endometrial carcinoma
Gastric cancer
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Blood protein levels C OR: 0.83 8E-14 PubMed
Other Variants in F2
rs62623459 rs121918477 rs121918478 rs121918479 rs121918480 rs121918481 rs121918482 rs387906522 rs1799963 rs121918483
Ask Dr. Hemsworth about this variant