rs569108

Variant in the MS4A2 gene (Membrane Spanning 4-Domains A2)

rs569108 is a single nucleotide polymorphism (SNP) in the MS4A2 gene, involved in mast cell activation. 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 rs569108 variant?

rs569108 is a SNP (single nucleotide polymorphism) in the MS4A2 (Membrane Spanning 4-Domains A2) gene. It belongs to the Adaptive Immunity category and is part of the Adaptive Immunity biological cluster. MS4A2 encodes FcεRIβ, the beta chain of the high-affinity IgE receptor on mast cells and basophils. It amplifies IgE-mediated signaling and variants are associated with atopic disease susceptibility.

Biological role and pathway

This variant sits within the MS4A2 gene, which is involved in the mast cell activation pathway. Genes within the Adaptive Immunity 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.

rs569108 and Long COVID / ME-CFS research

Mast cell activation syndrome (MCAS) is increasingly recognized in Long COVID, with symptoms of histamine excess including flushing, urticaria, GI disturbance, and cardiovascular instability. MS4A2 variants affecting mast cell IgE receptor sensitivity may contribute to MCAS-like features in Long COVID.

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

Parent gene: MS4A2

rs569108 is one of 3 known variants in the MS4A2 gene. To understand the full biological context of this variant, explore the parent gene page.

View MS4A2 gene page →

Conditions studied in relation to rs569108

Research into MS4A2 variants including rs569108 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 MS4A2 and the rs569108 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 MS4A2 gene

The following variants in MS4A2 are also studied in relation to chronic illness and may be analysed together for a more complete picture.

Frequently asked questions

What is the rs569108 variant in the MS4A2 gene?

rs569108 is a single nucleotide polymorphism (SNP) located in the MS4A2 (Membrane Spanning 4-Domains A2) gene, which is involved in mast cell activation. MS4A2 encodes FcεRIβ, the beta chain of the high-affinity IgE receptor on mast cells and basophils. It amplifies IgE-mediated signaling and variants are associated with atopic disease susceptibility.

How may the rs569108 variant relate to Long COVID or ME/CFS?

Mast cell activation syndrome (MCAS) is increasingly recognized in Long COVID, with symptoms of histamine excess including flushing, urticaria, GI disturbance, and cardiovascular instability. MS4A2 variants affecting mast cell IgE receptor sensitivity may contribute to MCAS-like features in Long COVID.

Can a consumer DNA test detect the rs569108 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.

Related articles

Find out if you carry the rs569108 variant

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References

The following publications were used in compiling the research context for MS4A2 and its variants. This is not an exhaustive literature review.

  • [1]PMID: 29548640
  • [2]Journal of Allergy and Clinical Immunology
  • [3]Nature Immunology