rs2978881

Variant in the GSR gene (Glutathione-Disulfide Reductase)

rs2978881 is a single nucleotide polymorphism (SNP) in the GSR gene, involved in glutathione recycling. 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 rs2978881 variant?

rs2978881 is a SNP (single nucleotide polymorphism) in the GSR (Glutathione-Disulfide Reductase) gene. It belongs to the Oxidative Stress category and is part of the Oxidative Stress biological cluster. GSR encodes glutathione reductase, which regenerates reduced glutathione from oxidized glutathione using NADPH.

Biological role and pathway

This variant sits within the GSR gene, which is involved in the glutathione recycling 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.

rs2978881 and Long COVID / ME-CFS research

GSR activity is essential for maintaining the glutathione pool; variants reducing GSR activity may amplify oxidative stress in Long COVID.

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

Parent gene: GSR

rs2978881 is one of 1 known variant in the GSR gene. To understand the full biological context of this variant, explore the parent gene page.

View GSR gene page →

Conditions studied in relation to rs2978881

Research into GSR variants including rs2978881 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 GSR and the rs2978881 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 rs2978881 variant in the GSR gene?

rs2978881 is a single nucleotide polymorphism (SNP) located in the GSR (Glutathione-Disulfide Reductase) gene, which is involved in glutathione recycling. GSR encodes glutathione reductase, which regenerates reduced glutathione from oxidized glutathione using NADPH.

How may the rs2978881 variant relate to Long COVID or ME/CFS?

GSR activity is essential for maintaining the glutathione pool; variants reducing GSR activity may amplify oxidative stress in Long COVID.

Can a consumer DNA test detect the rs2978881 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 rs2978881 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 GSR and its variants. This is not an exhaustive literature review.

  • [1]PMID: 25122754
  • [2]Nature Genetics
  • [3]Journal of Clinical Investigation