rs566926

Variant in the WNT5A gene (Wnt Family Member 5A)

rs566926 is a single nucleotide polymorphism (SNP) in the WNT5A gene, involved in non-canonical Wnt signaling / inflammation. 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 rs566926 variant?

rs566926 is a SNP (single nucleotide polymorphism) in the WNT5A (Wnt Family Member 5A) gene. It belongs to the Signaling category and is part of the Immune System & Inflammation biological cluster. WNT5A encodes a Wnt ligand that activates non-canonical Wnt/ROR2 signaling, promoting macrophage inflammatory activation.

Biological role and pathway

This variant sits within the WNT5A gene, which is involved in the non-canonical Wnt signaling / inflammation pathway. 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 — particularly under conditions of physiological stress such as viral infection or prolonged illness.

rs566926 and Long COVID / ME-CFS research

WNT5A drives macrophage pro-inflammatory activation; elevated WNT5A in COVID-19 may contribute to macrophage hyperactivation and the inflammatory milieu of Long COVID.

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

Parent gene: WNT5A

rs566926 is one of 1 known variant in the WNT5A gene. To understand the full biological context of this variant, explore the parent gene page.

View WNT5A gene page →

Conditions studied in relation to rs566926

Research into WNT5A variants including rs566926 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 WNT5A and the rs566926 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 rs566926 variant in the WNT5A gene?

rs566926 is a single nucleotide polymorphism (SNP) located in the WNT5A (Wnt Family Member 5A) gene, which is involved in non-canonical Wnt signaling / inflammation. WNT5A encodes a Wnt ligand that activates non-canonical Wnt/ROR2 signaling, promoting macrophage inflammatory activation.

How may the rs566926 variant relate to Long COVID or ME/CFS?

WNT5A drives macrophage pro-inflammatory activation; elevated WNT5A in COVID-19 may contribute to macrophage hyperactivation and the inflammatory milieu of Long COVID.

Can a consumer DNA test detect the rs566926 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 rs566926 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 WNT5A and its variants. This is not an exhaustive literature review.

  • [1]PMID: 32296168
  • [2]Nature Genetics
  • [3]Nature Immunology