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Currently, there is a need for a comprehensive assessment of the state of the hemostasis system in deeply premature newborns, including not only an assessment of the state of the vascular wall, platelet and plasma links of hemostasis, as well as the identification of features of polymorphism of genes controlling hemostasis. The identification of these features will help in predicting the development of hemorrhagic disorders in deeply premature newborns, which will make it possible to personalize the management tactics of this category of patients and reduce the rates of disability and infant mortality. In order to identify variants of polymorphism of genes of the hemostasis system in deeply premature newborns, a genetic examination of 99 children with a gestation period of up to 32 weeks was performed. With the definition of gene polymorphism: F2, F7, F13A1, FGB, ITGA2-a2, ITGB3-b3, PAI1. The study established combined variants of hemostasis gene polymorphism in children with hemorrhagic disorders, which can serve as a predictor of the formation of disorders in the hemostasis system.