Majority of high-risk profiles (24/33) were abnormally low haptoglobin (hemolysis or anhaptoglobinemia), 4 subjects had abnormally high apoA1 value, 1 abnormally low ApoA1, 2 abnormally high GGT, one Gilbert syndrome with 72 micromol of unconjugated bilirubin, and one abnormally high A2 M. The gene discussed is APOA1; the disease is anhaptoglobinemia.