rs5744068
Variant in the IL18R1 gene (Interleukin 18 Receptor 1)
rs5744068 is a single nucleotide polymorphism (SNP) in the IL18R1 gene, involved in IL-18 signaling / NK and T cell 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 rs5744068 variant?
rs5744068 is a SNP (single nucleotide polymorphism) in the IL18R1 (Interleukin 18 Receptor 1) gene. It belongs to the Immune Signaling category and is part of the Immune System & Inflammation biological cluster. IL18R1 encodes the primary signaling receptor for IL-18 on NK cells and T cells.
Biological role and pathway
This variant sits within the IL18R1 gene, which is involved in the IL-18 signaling / NK and T cell 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.
rs5744068 and Long COVID / ME-CFS research
IL18R1 variants affecting IL-18 signaling may modulate NK cell activation and IFN-gamma production relevant to the immune dysregulation of Long COVID.
This information is based on published research and does not constitute medical advice. See references below.
Parent gene: IL18R1
rs5744068 is one of 1 known variant in the IL18R1 gene. To understand the full biological context of this variant, explore the parent gene page.
View IL18R1 gene page →Conditions studied in relation to rs5744068
Research into IL18R1 variants including rs5744068 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 IL18R1 and the rs5744068 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 rs5744068 variant in the IL18R1 gene?
rs5744068 is a single nucleotide polymorphism (SNP) located in the IL18R1 (Interleukin 18 Receptor 1) gene, which is involved in IL-18 signaling / NK and T cell activation. IL18R1 encodes the primary signaling receptor for IL-18 on NK cells and T cells.
How may the rs5744068 variant relate to Long COVID or ME/CFS?
IL18R1 variants affecting IL-18 signaling may modulate NK cell activation and IFN-gamma production relevant to the immune dysregulation of Long COVID.
Can a consumer DNA test detect the rs5744068 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 rs5744068 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 IL18R1 and its variants. This is not an exhaustive literature review.
- [1]PMID: 33398161
- [2]Nature Genetics
- [3]Journal of Immunology