Non-significant, decreased risks associated with the rs696217 (OR 0.61-0.63, p = 0.09-0.11) GHRL polymorphism in breast, colorectal, esophageal and colorectal cancer were not altered when analyses were confined to breast cancer studies alone (OR 0.82-0.83, p = 0.57-0.60) (Table 2). The gene discussed is GHRL; the disease is colorectal cancer.