RS149067268 F5

Health Risk Chr 1:169542222
Upload your DNA to see your genotype for this variant.
Associated Conditions
Budd-Chiari syndrome
Factor V deficiency
Congenital factor V deficiency
Thrombophilia due to thrombin defect
Inborn genetic diseases
Budd-Chiari syndrome
Factor V deficiency
Congenital factor V deficiency
Thrombophilia due to thrombin defect
Inborn genetic diseases
Other Variants in F5
rs6025 rs118203905 rs118203906 rs118203912 rs2101818393 rs773569662 rs2101829195 rs118203907 rs118203908 rs118203909
Ask Dr. Hemsworth about this variant