RS200269019 F5

Health Risk Chr 1:169541869
Upload your DNA to see your genotype for this variant.
Associated Conditions
Inborn genetic diseases
Congenital factor V deficiency
Thrombophilia due to activated protein C resistance
Budd-Chiari syndrome
Ischemic stroke
Pregnancy loss
recurrent
susceptibility to
1
Inborn genetic diseases
Congenital factor V deficiency
Thrombophilia due to activated protein C resistance
Budd-Chiari syndrome
Ischemic stroke
Pregnancy loss
Other Variants in F5
rs6025 rs118203905 rs118203906 rs118203912 rs2101818393 rs773569662 rs2101829195 rs118203907 rs118203908 rs118203909
Ask Dr. Hemsworth about this variant