Genetic Risks and Predispositions

Integrin alpha-2 (platelet glycoprotein Ia/IIa) (ITGA2). Detection of mutation C807T (protein synthesis disorder)

Potassium Channel (KCNJ11). Detection of Mutation C67T (Lys23Gln)

Fibrinogen, beta polypeptide (FGB). Detection of G(-455)A mutation (gene regulatory region)

Blood Coagulation Factor 7 (F7). Detection of Mutation G10976A (Arg353Gln)

Guanine nucleotide-binding protein beta-3 (GNB3). Detection of C825T (Ser275Ser) mutation

Blood Coagulation Factor 2, Prothrombin (F2). Detection of G20210A Mutation (Gene Regulatory Region)

Adducin 1 (alpha) (ADD1). Detection of G1378T (Gly460Trp) mutation

Angiotensin II receptor type 2 (AGTR2). Detection of G1675A mutation (gene regulatory region)

Blood Coagulation Factor 5 (F5). Detection of G1691A (Arg506Gln) Mutation

Complement Factor H (CFH), C1204T (Tyr402His) Mutation Detection