rs713041
Variant in the GPX4 gene (Glutathione Peroxidase 4)
rs713041 is a single nucleotide polymorphism (SNP) in the GPX4 gene, involved in phospholipid hydroperoxide reduction / ferroptosis. 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 rs713041 variant?
rs713041 is a SNP (single nucleotide polymorphism) in the GPX4 (Glutathione Peroxidase 4) gene. It belongs to the Oxidative Stress category and is part of the Oxidative Stress biological cluster. GPX4 encodes glutathione peroxidase 4, which reduces phospholipid hydroperoxides and protects against ferroptosis.
Biological role and pathway
This variant sits within the GPX4 gene, which is involved in the phospholipid hydroperoxide reduction / ferroptosis pathway. Genes within the Oxidative Stress 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.
rs713041 and Long COVID / ME-CFS research
GPX4 prevents ferroptosis (iron-dependent cell death); reduced GPX4 activity may contribute to cell death and tissue damage in Long COVID, particularly in iron dysregulation states.
This information is based on published research and does not constitute medical advice. See references below.
Parent gene: GPX4
rs713041 is one of 1 known variant in the GPX4 gene. To understand the full biological context of this variant, explore the parent gene page.
View GPX4 gene page →Conditions studied in relation to rs713041
Research into GPX4 variants including rs713041 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 GPX4 and the rs713041 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 rs713041 variant in the GPX4 gene?
rs713041 is a single nucleotide polymorphism (SNP) located in the GPX4 (Glutathione Peroxidase 4) gene, which is involved in phospholipid hydroperoxide reduction / ferroptosis. GPX4 encodes glutathione peroxidase 4, which reduces phospholipid hydroperoxides and protects against ferroptosis.
How may the rs713041 variant relate to Long COVID or ME/CFS?
GPX4 prevents ferroptosis (iron-dependent cell death); reduced GPX4 activity may contribute to cell death and tissue damage in Long COVID, particularly in iron dysregulation states.
Can a consumer DNA test detect the rs713041 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 rs713041 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 GPX4 and its variants. This is not an exhaustive literature review.
- [1]PMID: 34088393
- [2]Nature Genetics
- [3]Cell