HapMap

The HapMap (Haplotype Map) is a research project that maps common genetic variations across the human genome. It identifies patterns of inherited DNA segments, called haplotypes, which are shared among people. This helps scientists understand how genetic differences relate to health, disease risk, and drug response. By providing a detailed map of these variations, the HapMap accelerates genetic research and personalized medicine, making it easier to study the genetic factors that influence our characteristics and susceptibility to illnesses.