rs34550074

Variant in the EPX gene (Eosinophil Peroxidase)

rs34550074 is a single nucleotide polymorphism (SNP) in the EPX gene, involved in eosinophil antimicrobial defense / oxidative. 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 rs34550074 variant?

rs34550074 is a SNP (single nucleotide polymorphism) in the EPX (Eosinophil Peroxidase) gene. It belongs to the Immune Signaling category and is part of the Histamine & MCAS biological cluster. EPX encodes eosinophil peroxidase, which generates reactive oxygen species in eosinophil granules for antimicrobial defense.

Biological role and pathway

This variant sits within the EPX gene, which is involved in the eosinophil antimicrobial defense / oxidative pathway. Genes within the Histamine & MCAS 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.

rs34550074 and Long COVID / ME-CFS research

Eosinophil degranulation and EPX-derived oxidants contribute to airway inflammation; eosinopenia in acute COVID-19 followed by eosinophilia in some Long COVID patients may be influenced by EPX variants.

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

Parent gene: EPX

rs34550074 is one of 1 known variant in the EPX gene. To understand the full biological context of this variant, explore the parent gene page.

View EPX gene page →

Conditions studied in relation to rs34550074

Research into EPX variants including rs34550074 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 EPX and the rs34550074 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 rs34550074 variant in the EPX gene?

rs34550074 is a single nucleotide polymorphism (SNP) located in the EPX (Eosinophil Peroxidase) gene, which is involved in eosinophil antimicrobial defense / oxidative. EPX encodes eosinophil peroxidase, which generates reactive oxygen species in eosinophil granules for antimicrobial defense.

How may the rs34550074 variant relate to Long COVID or ME/CFS?

Eosinophil degranulation and EPX-derived oxidants contribute to airway inflammation; eosinopenia in acute COVID-19 followed by eosinophilia in some Long COVID patients may be influenced by EPX variants.

Can a consumer DNA test detect the rs34550074 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 rs34550074 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 EPX and its variants. This is not an exhaustive literature review.

  • [1]PMID: 33398161
  • [2]Nature Genetics
  • [3]Journal of Allergy and Clinical Immunology