GENETIC TESTING

Coagulation disorders

Faktor V Leiden

Prothrombin 20210 G>A

Factor XIII V34L

Fibrinogen gamma 10034C>T

PAI1 4G/5G

Hyperhomocysteinemia (MTHFR 677C>T)

Metabolic disorders

Hereditary hemochromatosis

Lactose intolerance

Hereditary fructose intolerance

Alpha1-antitrypsin deficiency

Morbus Wilson (ATP7B)

Dyslipidemia

ApoB100 R3500Q

ApoE genotyping

Pharmakogenetic

5-FU toxicity (DPYD)

Thiopurin toxicity (TPMT)

Warfarin sensitivity (VKORC1, CYP2C9)

Clopidogrel resistance (CYP2C19)

Statin side effects (SLCO1B1)

Tamoxifen sensitivity (CYP2D6)

Methotrexate toxicity (MTHFR)

Autoimmune diseases

HLA-B27

Celaic disease (HLA-DQA1, HLAD-DQB1)

Miscellaneous

Age-related macular degeneration (CFH)

Familial mediterranean fever (MEFV)