Genetic Risks and Predispositions

Endothelial nitric oxide synthase (NOS3). Detection of G894T (Glu298Asp) mutation

Integrin beta-3 (platelet fibrinogen receptor beta subunit) (ITGB3). Detection of T1565C (Leu59Pro) mutation

Angiotensin II Receptor Type 1 (AGTR1). Detection of A1166C Mutation (Gene Regulatory Region)

Angiotensinogen (AGT). Detection of T704C (Met235Thr) mutation

Endothelial nitric oxide synthase (NOS3). Detection of T(-786)C mutation (gene regulatory region)

Beta-2 adrenergic receptor (ADRB2). Detection of G46A (Arg16Gly) mutation

Age-Related Maculopathy Susceptibility 2 Gene (ARMS2). Detection of Mutation G205T (Ala69Ser)

Interleukin 1B (IL1B). Detection of C3953T mutation (protein synthesis disorder)

Interleukin 1A (IL1A). Detection of mutation C(-889)T (gene regulatory region)

Apolipoprotein E (ApoE). Detection of e2-e3-e4 polymorphism