ITGB3 Gene
Integrin Subunit Beta 3 (ITGB3) is a gene involved in platelet aggregation that has been studied in relation to immune function, metabolism, and chronic illness. Variants in ITGB3 may influence how the body responds to infection, inflammation, and long-term recovery.
This page is for educational and informational purposes only. Not a diagnostic tool. Always consult a qualified healthcare provider.
What is the ITGB3 gene?
ITGB3 encodes integrin subunit beta 3, a protein involved in platelet aggregation. It belongs to the Coagulation category and is part of the Coagulation & Vascular biological cluster. ITGB3 forms αIIbβ3 (GPIIb-IIIa) on platelets — the most abundant platelet surface protein and the final common pathway for platelet aggregation through fibrinogen binding. The PlA2 (Leu33Pro, rs5918) variant affects thrombotic risk.
Biological role and pathway
ITGB3 is involved in the platelet aggregation pathway, which plays a central role in regulating physiological processes relevant to immune defence, cellular energy, and systemic homeostasis. Genes within the Coagulation & Vascular cluster work together to maintain balanced function across interconnected biological systems.
Variants in genes within this pathway may influence an individual's predisposition to altered function in these systems — particularly under conditions of physiological stress such as viral infection or prolonged illness.
ITGB3 and Long COVID / ME-CFS research
αIIbβ3 mediates fibrinogen-dependent platelet aggregation in COVID-19 microthrombi. ITGB3 PlA2 (rs5918) is associated with increased platelet aggregation and thrombotic risk; this variant may modulate the severity of platelet-fibrin microthrombi in Long COVID vascular disease.
This information is based on published research and does not constitute medical advice. See references below.
Known genetic variants
The following variants (SNPs) in the ITGB3 gene have been studied in relation to coagulation and chronic illness. Each variant represents a single nucleotide position where individuals may carry different alleles.
Conditions studied in relation to ITGB3
Research into ITGB3 variants has explored associations with the following conditions. These are areas of scientific investigation and do not imply that ITGB3 causes or treats any condition.
Genetic insights from DNA data
Consumer DNA files from 23andMe, AncestryDNA, and MyHeritage contain raw SNP data. When you upload your file to ChronicDNA, the analysis engine checks your genotype against a curated panel of 80+ genes selected for their relevance to Long COVID, ME/CFS, and connected biological pathways - some of which may include ITGB3 and related genes in the coagulation & vascular pathway.
The report is educational - it explains which variants you carry, what the research says about them, and how they fit into the biological pathways most relevant to chronic illness. Results are presented in plain English with appropriate scientific context, no medical jargon, no scare tactics. All results should be discussed with a qualified healthcare provider.
Related genes in the Coagulation & Vascular pathway
ITGB3 does not act in isolation. The following genes are functionally related and may be analysed together for a more complete picture of your genetic predispositions.
Frequently asked questions
What is the ITGB3 gene and what does it do?
ITGB3 (Integrin Subunit Beta 3) is involved in platelet aggregation. ITGB3 forms αIIbβ3 (GPIIb-IIIa) on platelets — the most abundant platelet surface protein and the final common pathway for platelet aggregation through fibrinogen binding. The PlA2 (Leu33Pro, rs5918) variant affects thrombotic risk.
How may ITGB3 gene variants relate to Long COVID or ME/CFS?
αIIbβ3 mediates fibrinogen-dependent platelet aggregation in COVID-19 microthrombi. ITGB3 PlA2 (rs5918) is associated with increased platelet aggregation and thrombotic risk; this variant may modulate the severity of platelet-fibrin microthrombi in Long COVID vascular disease.
Can a DNA test reveal information about my ITGB3 gene?
Consumer DNA data from 23andMe, AncestryDNA, and MyHeritage includes SNP variants for many genes. ChronicDNA analyses your raw DNA file and reports on variants that have been studied in relation to chronic illness, immune function, and metabolism. This is not a diagnostic service — results are informational and educational only.
Explore your ITGB3 genetic insights
Upload your DNA data from 23andMe, AncestryDNA, or MyHeritage and receive a personalised report covering >80 genes relevant to Long COVID and ME/CFS.
Get Your Personalised DNA ReportInformational and educational only · Not a diagnostic tool · GDPR compliant
References
The following publications were used in compiling the research context for ITGB3. This is not an exhaustive literature review.
- [1]PMID: 27568270
- [2]Blood
- [3]New England Journal of Medicine