rs2430561
Variant in the IFNG gene (Interferon Gamma)
rs2430561 is a single nucleotide polymorphism (SNP) in the IFNG gene, involved in interferon 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 rs2430561 variant?
rs2430561 is a SNP (single nucleotide polymorphism) in the IFNG (Interferon Gamma) gene. It belongs to the Immune Signaling category and is part of the Immune System & Inflammation biological cluster. IFNG encodes interferon gamma, a critical cytokine for antiviral immunity and macrophage activation.
Biological role and pathway
This variant sits within the IFNG gene, which is involved in the interferon signaling 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.
rs2430561 and Long COVID / ME-CFS research
Aberrant IFNG production has been studied in relation to persistent immune activation and T cell exhaustion in Long COVID.
This information is based on published research and does not constitute medical advice. See references below.
Parent gene: IFNG
rs2430561 is one of 1 known variant in the IFNG gene. To understand the full biological context of this variant, explore the parent gene page.
View IFNG gene page →Conditions studied in relation to rs2430561
Research into IFNG variants including rs2430561 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 IFNG and the rs2430561 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 rs2430561 variant in the IFNG gene?
rs2430561 is a single nucleotide polymorphism (SNP) located in the IFNG (Interferon Gamma) gene, which is involved in interferon signaling. IFNG encodes interferon gamma, a critical cytokine for antiviral immunity and macrophage activation.
How may the rs2430561 variant relate to Long COVID or ME/CFS?
Aberrant IFNG production has been studied in relation to persistent immune activation and T cell exhaustion in Long COVID.
Can a consumer DNA test detect the rs2430561 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 rs2430561 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 ReportInformational and educational only · Not a diagnostic tool · GDPR compliant
References
The following publications were used in compiling the research context for IFNG and its variants. This is not an exhaustive literature review.
- [1]PMID: 32972995
- [2]Nature Genetics
- [3]Journal of Clinical Investigation