rs11171739
Variant in the IL25 gene (Interleukin 25 (IL-17E))
rs11171739 is a single nucleotide polymorphism (SNP) in the IL25 gene, involved in barrier immunity and Th2 amplification. 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 rs11171739 variant?
rs11171739 is a SNP (single nucleotide polymorphism) in the IL25 (Interleukin 25 (IL-17E)) gene. It belongs to the Immune Signaling category and is part of the Cytokines & Immune Signaling biological cluster. IL25 encodes IL-17E, an alarmin released by barrier epithelial cells that amplifies Th2 responses and mast cell activation.
Biological role and pathway
This variant sits within the IL25 gene, which is involved in the barrier immunity and Th2 amplification pathway. Genes within the Cytokines & Immune Signaling 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.
rs11171739 and Long COVID / ME-CFS research
IL25 release from damaged mucosal epithelium may amplify allergic-type immune responses in Long COVID patients.
This information is based on published research and does not constitute medical advice. See references below.
Parent gene: IL25
rs11171739 is one of 1 known variant in the IL25 gene. To understand the full biological context of this variant, explore the parent gene page.
View IL25 gene page →Conditions studied in relation to rs11171739
Research into IL25 variants including rs11171739 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 IL25 and the rs11171739 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.
Other variants in the IL25 gene
The following variants in IL25 are also studied in relation to chronic illness and may be analysed together for a more complete picture.
Frequently asked questions
What is the rs11171739 variant in the IL25 gene?
rs11171739 is a single nucleotide polymorphism (SNP) located in the IL25 (Interleukin 25 (IL-17E)) gene, which is involved in barrier immunity and Th2 amplification. IL25 encodes IL-17E, an alarmin released by barrier epithelial cells that amplifies Th2 responses and mast cell activation.
How may the rs11171739 variant relate to Long COVID or ME/CFS?
IL25 release from damaged mucosal epithelium may amplify allergic-type immune responses in Long COVID patients.
Can a consumer DNA test detect the rs11171739 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 rs11171739 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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References
The following publications were used in compiling the research context for IL25 and its variants. This is not an exhaustive literature review.
- [1]PMID: 34316049
- [2]Nature Genetics
- [3]Journal of Clinical Investigation