rs34516001

Variant in the PRDX1 gene (Peroxiredoxin 1)

rs34516001 is a single nucleotide polymorphism (SNP) in the PRDX1 gene, involved in hydrogen peroxide reduction. 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 rs34516001 variant?

rs34516001 is a SNP (single nucleotide polymorphism) in the PRDX1 (Peroxiredoxin 1) gene. It belongs to the Oxidative Stress category and is part of the Oxidative Stress biological cluster. PRDX1 encodes a thioredoxin-dependent peroxidase that reduces hydrogen peroxide and organic hydroperoxides in the cytoplasm.

Biological role and pathway

This variant sits within the PRDX1 gene, which is involved in the hydrogen peroxide reduction 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.

rs34516001 and Long COVID / ME-CFS research

Peroxiredoxin activity protects cells from oxidative damage; variants may affect redox homeostasis in Long COVID-associated fatigue and inflammation.

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

Parent gene: PRDX1

rs34516001 is one of 1 known variant in the PRDX1 gene. To understand the full biological context of this variant, explore the parent gene page.

View PRDX1 gene page →

Conditions studied in relation to rs34516001

Research into PRDX1 variants including rs34516001 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 PRDX1 and the rs34516001 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 rs34516001 variant in the PRDX1 gene?

rs34516001 is a single nucleotide polymorphism (SNP) located in the PRDX1 (Peroxiredoxin 1) gene, which is involved in hydrogen peroxide reduction. PRDX1 encodes a thioredoxin-dependent peroxidase that reduces hydrogen peroxide and organic hydroperoxides in the cytoplasm.

How may the rs34516001 variant relate to Long COVID or ME/CFS?

Peroxiredoxin activity protects cells from oxidative damage; variants may affect redox homeostasis in Long COVID-associated fatigue and inflammation.

Can a consumer DNA test detect the rs34516001 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 rs34516001 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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Informational and educational only · Not a diagnostic tool · GDPR compliant

References

The following publications were used in compiling the research context for PRDX1 and its variants. This is not an exhaustive literature review.

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