FGB Gene
Fibrinogen Beta Chain (FGB) is a gene involved in fibrin formation that has been studied in relation to immune function, metabolism, and chronic illness. Variants in FGB 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 FGB gene?
FGB encodes fibrinogen beta chain, a protein involved in fibrin formation. It belongs to the Coagulation category and is part of the Coagulation & Vascular biological cluster. FGB encodes the beta chain of fibrinogen. The FGB promoter variant -455G>A (rs1800790) increases fibrinogen plasma levels and is associated with cardiovascular disease risk. Fibrinogen beta also participates in platelet-fibrinogen interactions.
Biological role and pathway
FGB is involved in the fibrin formation 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.
FGB and Long COVID / ME-CFS research
Elevated fibrinogen levels in Long COVID patients may reflect both acute phase response and procoagulant states. FGB -455G>A increases baseline fibrinogen levels, potentially contributing to hypercoagulability and the fibrin microclot burden in Long COVID.
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 FGB 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 FGB
Research into FGB variants has explored associations with the following conditions. These are areas of scientific investigation and do not imply that FGB 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 FGB 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
FGB 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 FGB gene and what does it do?
FGB (Fibrinogen Beta Chain) is involved in fibrin formation. FGB encodes the beta chain of fibrinogen. The FGB promoter variant -455G>A (rs1800790) increases fibrinogen plasma levels and is associated with cardiovascular disease risk. Fibrinogen beta also participates in platelet-fibrinogen interactions.
How may FGB gene variants relate to Long COVID or ME/CFS?
Elevated fibrinogen levels in Long COVID patients may reflect both acute phase response and procoagulant states. FGB -455G>A increases baseline fibrinogen levels, potentially contributing to hypercoagulability and the fibrin microclot burden in Long COVID.
Can a DNA test reveal information about my FGB 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 FGB 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 FGB. This is not an exhaustive literature review.
- [1]PMID: 26785756
- [2]Blood
- [3]Arteriosclerosis Thrombosis and Vascular Biology