rs1634517

Variant in the CCL4 gene (C-C Motif Chemokine Ligand 4 (MIP-1-beta))

rs1634517 is a single nucleotide polymorphism (SNP) in the CCL4 gene, involved in macrophage and T cell recruitment. 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 rs1634517 variant?

rs1634517 is a SNP (single nucleotide polymorphism) in the CCL4 (C-C Motif Chemokine Ligand 4 (MIP-1-beta)) gene. It belongs to the Chemokine category and is part of the Chemokines biological cluster. CCL4 encodes macrophage inflammatory protein-1 beta, a chemokine that attracts monocytes, NK cells, and T cells.

Biological role and pathway

This variant sits within the CCL4 gene, which is involved in the macrophage and T cell recruitment pathway. Genes within the Chemokines 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.

rs1634517 and Long COVID / ME-CFS research

CCL4 drives immune cell recruitment and activation; elevated levels may reflect persistent macrophage and lymphocyte trafficking in Long COVID.

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

Parent gene: CCL4

rs1634517 is one of 1 known variant in the CCL4 gene. To understand the full biological context of this variant, explore the parent gene page.

View CCL4 gene page →

Conditions studied in relation to rs1634517

Research into CCL4 variants including rs1634517 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 CCL4 and the rs1634517 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 rs1634517 variant in the CCL4 gene?

rs1634517 is a single nucleotide polymorphism (SNP) located in the CCL4 (C-C Motif Chemokine Ligand 4 (MIP-1-beta)) gene, which is involved in macrophage and T cell recruitment. CCL4 encodes macrophage inflammatory protein-1 beta, a chemokine that attracts monocytes, NK cells, and T cells.

How may the rs1634517 variant relate to Long COVID or ME/CFS?

CCL4 drives immune cell recruitment and activation; elevated levels may reflect persistent macrophage and lymphocyte trafficking in Long COVID.

Can a consumer DNA test detect the rs1634517 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 rs1634517 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 CCL4 and its variants. This is not an exhaustive literature review.

  • [1]PMID: 33153018
  • [2]Nature Genetics
  • [3]Journal of Clinical Investigation