rs34713741

Variant in the SELENOS gene (Selenoprotein S)

rs34713741 is a single nucleotide polymorphism (SNP) in the SELENOS gene, involved in ER stress / selenoprotein. 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 rs34713741 variant?

rs34713741 is a SNP (single nucleotide polymorphism) in the SELENOS (Selenoprotein S) gene. It belongs to the Oxidative Stress category and is part of the Oxidative Stress biological cluster. SELENOS encodes selenoprotein S, an ER-resident selenoprotein involved in ER stress responses and inflammatory signaling.

Biological role and pathway

This variant sits within the SELENOS gene, which is involved in the ER stress / selenoprotein 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.

rs34713741 and Long COVID / ME-CFS research

Selenium status affects selenoprotein expression; SELENOS variants may influence ER stress responses and the inflammatory cytokine production relevant to Long COVID.

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

Parent gene: SELENOS

rs34713741 is one of 2 known variants in the SELENOS gene. To understand the full biological context of this variant, explore the parent gene page.

View SELENOS gene page →

Conditions studied in relation to rs34713741

Research into SELENOS variants including rs34713741 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 SELENOS and the rs34713741 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.

Other variants in the SELENOS gene

The following variants in SELENOS are also studied in relation to chronic illness and may be analysed together for a more complete picture.

Frequently asked questions

What is the rs34713741 variant in the SELENOS gene?

rs34713741 is a single nucleotide polymorphism (SNP) located in the SELENOS (Selenoprotein S) gene, which is involved in ER stress / selenoprotein. SELENOS encodes selenoprotein S, an ER-resident selenoprotein involved in ER stress responses and inflammatory signaling.

How may the rs34713741 variant relate to Long COVID or ME/CFS?

Selenium status affects selenoprotein expression; SELENOS variants may influence ER stress responses and the inflammatory cytokine production relevant to Long COVID.

Can a consumer DNA test detect the rs34713741 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 rs34713741 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 SELENOS and its variants. This is not an exhaustive literature review.

  • [1]PMID: 34088393
  • [2]Nature Genetics
  • [3]FASEB Journal