S100A8 Gene
S100 Calcium Binding Protein A8 (Calprotectin) (S100A8) is a gene involved in DAMP / neutrophil and macrophage inflammation that has been studied in relation to immune function, metabolism, and chronic illness. Variants in S100A8 may influence how the body responds to infection, inflammation, and long-term recovery.
This page is for educational and informational purposes only. Not a diagnostic tool. Always consult a qualified healthcare provider.
What is the S100A8 gene?
S100A8 encodes s100 calcium binding protein a8 (calprotectin), a protein involved in DAMP / neutrophil and macrophage inflammation. It belongs to the Immune Signaling category and is part of the Immune System & Inflammation biological cluster. S100A8 encodes a calcium-binding alarmin protein released by neutrophils and macrophages that amplifies inflammation via TLR4.
Biological role and pathway
S100A8 is involved in the DAMP / neutrophil and macrophage inflammation pathway, which plays a central role in regulating physiological processes relevant to immune defence, cellular energy, and systemic homeostasis. Genes within the Immune System & Inflammation 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 in these systems — particularly under conditions of physiological stress such as viral infection or prolonged illness.
S100A8 and Long COVID / ME-CFS research
S100A8/A9 (calprotectin) complex is massively elevated in COVID-19 cytokine storm and persists as a Long COVID biomarker; variants may affect innate immune alarm signal amplification.
This information is based on published research and does not constitute medical advice. See references below.
Known genetic variants
The following variants (SNPs) in the S100A8 gene have been studied in relation to immune signaling and chronic illness. Each variant represents a single nucleotide position where individuals may carry different alleles.
- rs3006488— S100A8 variant
Conditions studied in relation to S100A8
Research into S100A8 variants has explored associations with the following conditions. These are areas of scientific investigation and do not imply that S100A8 causes or treats any condition.
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 S100A8 and related genes in the immune system & inflammation pathway.
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.
Related genes in the Immune System & Inflammation pathway
S100A8 does not act in isolation. The following genes are functionally related and may be analysed together for a more complete picture of your genetic predispositions.
Frequently asked questions
What is the S100A8 gene and what does it do?
S100A8 (S100 Calcium Binding Protein A8 (Calprotectin)) is involved in DAMP / neutrophil and macrophage inflammation. S100A8 encodes a calcium-binding alarmin protein released by neutrophils and macrophages that amplifies inflammation via TLR4.
How may S100A8 gene variants relate to Long COVID or ME/CFS?
S100A8/A9 (calprotectin) complex is massively elevated in COVID-19 cytokine storm and persists as a Long COVID biomarker; variants may affect innate immune alarm signal amplification.
Can a DNA test reveal information about my S100A8 gene?
Consumer DNA data from 23andMe, AncestryDNA, and MyHeritage includes SNP variants for many genes. ChronicDNA analyses your raw DNA file and reports on variants that have been studied in relation to chronic illness, immune function, and metabolism. This is not a diagnostic service — results are informational and educational only.
Explore your S100A8 genetic insights
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 ReportInformational and educational only · Not a diagnostic tool · GDPR compliant
References
The following publications were used in compiling the research context for S100A8. This is not an exhaustive literature review.
- [1]PMID: 32296168
- [2]Nature Medicine
- [3]Cell