The "T Allele" refers to a specific variant of a gene that can influence various traits in organisms, including humans. Alleles are different forms of a gene that arise through mutation and can result in variations in physical characteristics or disease susceptibility. The T Allele is often studied in genetics to understand its role in inheritance and phenotypic expression. In the context of human genetics, the T Allele can be associated with certain health conditions or traits, such as blood type or response to medications. Researchers analyze the presence of the T Allele to gain insights into genetic predispositions and to develop personalized medicine approaches.