rs2232582

Variant in the LBP gene (Lipopolysaccharide Binding Protein)

rs2232582 is a single nucleotide polymorphism (SNP) in the LBP gene, involved in LPS detection / innate immune activation. Variants at this position have been studied in relation to immune function, metabolism, and chronic illness.

This page is for educational and informational purposes only. Not a diagnostic tool. Always consult a qualified healthcare provider.

What is the rs2232582 variant?

rs2232582 is a SNP (single nucleotide polymorphism) in the LBP (Lipopolysaccharide Binding Protein) gene. It belongs to the Immune Signaling category and is part of the Immune System & Inflammation biological cluster. LBP encodes lipopolysaccharide-binding protein, which transfers LPS to CD14 to initiate TLR4-mediated macrophage activation.

Biological role and pathway

This variant sits within the LBP gene, which is involved in the LPS detection / innate immune activation pathway. Genes within the Immune System & Inflammation 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 — particularly under conditions of physiological stress such as viral infection or prolonged illness.

rs2232582 and Long COVID / ME-CFS research

LBP-mediated LPS delivery activates systemic innate immunity; elevated LBP in Long COVID patients reflects gut permeability and microbial translocation contributing to chronic inflammation.

This information is based on published research and does not constitute medical advice. See references below.

Parent gene: LBP

rs2232582 is one of 1 known variant in the LBP gene. To understand the full biological context of this variant, explore the parent gene page.

View LBP gene page →

Conditions studied in relation to rs2232582

Research into LBP variants including rs2232582 has explored associations with the following conditions. These are areas of scientific investigation and do not imply causation.

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 LBP and the rs2232582 variant.

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.

Frequently asked questions

What is the rs2232582 variant in the LBP gene?

rs2232582 is a single nucleotide polymorphism (SNP) located in the LBP (Lipopolysaccharide Binding Protein) gene, which is involved in LPS detection / innate immune activation. LBP encodes lipopolysaccharide-binding protein, which transfers LPS to CD14 to initiate TLR4-mediated macrophage activation.

How may the rs2232582 variant relate to Long COVID or ME/CFS?

LBP-mediated LPS delivery activates systemic innate immunity; elevated LBP in Long COVID patients reflects gut permeability and microbial translocation contributing to chronic inflammation.

Can a consumer DNA test detect the rs2232582 variant?

Many consumer DNA tests such as 23andMe, AncestryDNA, and MyHeritage genotype common SNPs. ChronicDNA analyses your raw DNA file and reports on variants studied in relation to chronic illness, immune function, and metabolism. This is not a diagnostic service — results are informational and educational only.

Find out if you carry the rs2232582 variant

Upload your DNA data from 23andMe, AncestryDNA, or MyHeritage and receive a personalised report covering >80 genes relevant to Long COVID and ME/CFS.

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Informational and educational only · Not a diagnostic tool · GDPR compliant

References

The following publications were used in compiling the research context for LBP and its variants. This is not an exhaustive literature review.

  • [1]PMID: 32296168
  • [2]Nature Genetics
  • [3]Journal of Infectious Diseases