rs10903323

Variant in the MSRA gene (Methionine Sulfoxide Reductase A)

rs10903323 is a single nucleotide polymorphism (SNP) in the MSRA gene, involved in protein oxidation repair. 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 rs10903323 variant?

rs10903323 is a SNP (single nucleotide polymorphism) in the MSRA (Methionine Sulfoxide Reductase A) gene. It belongs to the Oxidative Stress category and is part of the Oxidative Stress biological cluster. MSRA encodes methionine sulfoxide reductase A, which repairs oxidized methionine residues in proteins, counteracting oxidative damage.

Biological role and pathway

This variant sits within the MSRA gene, which is involved in the protein oxidation repair 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.

rs10903323 and Long COVID / ME-CFS research

MSRA activity protects proteins from oxidative modification; variants may affect protein quality and cellular function under Long COVID oxidative stress.

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

Parent gene: MSRA

rs10903323 is one of 1 known variant in the MSRA gene. To understand the full biological context of this variant, explore the parent gene page.

View MSRA gene page →

Conditions studied in relation to rs10903323

Research into MSRA variants including rs10903323 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 MSRA and the rs10903323 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 rs10903323 variant in the MSRA gene?

rs10903323 is a single nucleotide polymorphism (SNP) located in the MSRA (Methionine Sulfoxide Reductase A) gene, which is involved in protein oxidation repair. MSRA encodes methionine sulfoxide reductase A, which repairs oxidized methionine residues in proteins, counteracting oxidative damage.

How may the rs10903323 variant relate to Long COVID or ME/CFS?

MSRA activity protects proteins from oxidative modification; variants may affect protein quality and cellular function under Long COVID oxidative stress.

Can a consumer DNA test detect the rs10903323 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 rs10903323 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 MSRA and its variants. This is not an exhaustive literature review.

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