rs3811047

Variant in the IL37 gene (Interleukin 37)

rs3811047 is a single nucleotide polymorphism (SNP) in the IL37 gene, involved in anti-inflammatory cytokine signaling. 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 rs3811047 variant?

rs3811047 is a SNP (single nucleotide polymorphism) in the IL37 (Interleukin 37) gene. It belongs to the Immune Signaling category and is part of the Cytokines & Immune Signaling biological cluster. IL37 encodes a broadly anti-inflammatory cytokine that suppresses innate and adaptive immune responses via interleukin-18 receptor complex.

Biological role and pathway

This variant sits within the IL37 gene, which is involved in the anti-inflammatory cytokine signaling 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.

rs3811047 and Long COVID / ME-CFS research

IL37 has broad anti-inflammatory properties and may influence immune resolution; variants reducing IL37 activity may contribute to Long COVID chronicity.

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

Parent gene: IL37

rs3811047 is one of 1 known variant in the IL37 gene. To understand the full biological context of this variant, explore the parent gene page.

View IL37 gene page →

Conditions studied in relation to rs3811047

Research into IL37 variants including rs3811047 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 IL37 and the rs3811047 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 rs3811047 variant in the IL37 gene?

rs3811047 is a single nucleotide polymorphism (SNP) located in the IL37 (Interleukin 37) gene, which is involved in anti-inflammatory cytokine signaling. IL37 encodes a broadly anti-inflammatory cytokine that suppresses innate and adaptive immune responses via interleukin-18 receptor complex.

How may the rs3811047 variant relate to Long COVID or ME/CFS?

IL37 has broad anti-inflammatory properties and may influence immune resolution; variants reducing IL37 activity may contribute to Long COVID chronicity.

Can a consumer DNA test detect the rs3811047 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 rs3811047 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.

Get Your Personalised DNA Report

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

References

The following publications were used in compiling the research context for IL37 and its variants. This is not an exhaustive literature review.

  • [1]PMID: 34316049
  • [2]Nature Genetics
  • [3]Journal of Clinical Investigation