Sequence-based CLEC7A rs3901533 gene Polymorphisms Linked to Iraqi COVID-19 Patients | ||||
Egyptian Journal of Medical Microbiology | ||||
Article 2, Volume 35, Issue 1, January 2026 | ||||
Document Type: New and original researches in the field of Microbiology. | ||||
DOI: 10.21608/ejmm.2025.389814.1676 | ||||
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Authors | ||||
Ayad Abdelsalam ![]() | ||||
1Radiology Techniques Department, College of Health and Medical Techniques, Al-Mustaqbal University, 51001, Babylon, Iraq | ||||
2Medical Laboratory Techniques Department, College of Health and Medical Techniques, Al-Mustaqbal University, Babylon, 51001, Iraq. | ||||
3Environmental Health Department, College of Environmental Sciences, AL-Qasim Green University, Babylon, 51013, Iraq | ||||
Abstract | ||||
Background: The genetic diversity of the hosts may have an impact on the clinical range of COVID-19 severity. Dectin-1, an integral component of the innate immune response to SARS-CoV-2, is encoded by the CLEC7A gene. Objectives: This study investigates the relationship between Iraqi patients' susceptibility to COVID-19 and CLEC7A rs3901533 (A/C) polymorphisms. Methodology: Twenty COVID-19 patients, twenty recovered people, and twenty healthy controls provided a total of sixty DNA samples. Using the sequencing method, the CLEC7A rs3901533 (A/C) polymorphisms were genotyped. Results: The frequencies of the A and C alleles were 45%, 52.5%, and 55%, respectively, in patients, recovered individuals, and controls, and 57.5%, 47.5%, and 45%, respectively. Among COVID-19 patients, the CC genotype was much more common (30%) than in controls (15%), indicating a strong correlation with higher susceptibility to the disease (P-value < 0.05). Conclusion: According to the results, the CC genotype of the CLEC7A rs3901533 polymorphism may be a genetic risk factor for heightened susceptibility to COVID-19. These findings demonstrate the potential of CLEC7A genotyping in predicting the course of disease and directing individualised treatment strategies. | ||||
Keywords | ||||
COVID‐19; cytokines; SARS‐CoV‐2; CLEC7A rs3901533 | ||||
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