Coagulation disorders

• Factor V Leiden
• Prothrombin 20210 G>A
• Factor XIII V34L
• Fibrinogen gamma 10034C>T
• PAI-1 4G/5G
• Hyperhomocysteinemia (MTHFR 677C>T)

• Hereditary hemochromatosis
  
• Lactose intolerance
• Hereditary fructose intolerance
• Alpha1-antitrypsin deficiency
• Morbus Wilson (ATP7B)

• ApoB100 R3500Q
• ApoE genotyping
• Statin side effects (SLCO1B1)

• Collagen 1A1 (COL1A1)
• Lactose intolerance

• 5-FU toxicity (DPYD)
• Thiopurin toxicity (TPMT)
• Warfarin sensitivity (VKORC1, CYP2C9)
• Clopidogrel resistance (CYP2C19)
• Statin side effects (SLCO1B1)
• Tamoxifen sensitivity (CYP2D6)
• Methotrexate toxicity (MTHFR)

• HLA-B27
• Celaic disease (HLA-DQA1, HLAD-DQB1)

• Age-related macular degeneration (CFH)
• Familial mediterranean fever (MEFV)