rs2395471

Variant in the CD4 gene (CD4 Molecule)

rs2395471 is a single nucleotide polymorphism (SNP) in the CD4 gene, involved in MHC class II T cell signaling. 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 rs2395471 variant?

rs2395471 is a SNP (single nucleotide polymorphism) in the CD4 (CD4 Molecule) gene. It belongs to the Lymphocyte category and is part of the Lymphocyte Biology biological cluster. CD4 encodes the co-receptor for MHC class II, expressed on helper T cells and macrophages; also serves as a SARS-CoV-2 entry receptor.

Biological role and pathway

This variant sits within the CD4 gene, which is involved in the MHC class II T cell signaling pathway. Genes within the Lymphocyte Biology 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.

rs2395471 and Long COVID / ME-CFS research

CD4+ T cell depletion and exhaustion are associated with COVID-19 severity and may reflect impaired adaptive immunity in Long COVID.

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

Parent gene: CD4

rs2395471 is one of 1 known variant in the CD4 gene. To understand the full biological context of this variant, explore the parent gene page.

View CD4 gene page →

Conditions studied in relation to rs2395471

Research into CD4 variants including rs2395471 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 CD4 and the rs2395471 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 rs2395471 variant in the CD4 gene?

rs2395471 is a single nucleotide polymorphism (SNP) located in the CD4 (CD4 Molecule) gene, which is involved in MHC class II T cell signaling. CD4 encodes the co-receptor for MHC class II, expressed on helper T cells and macrophages; also serves as a SARS-CoV-2 entry receptor.

How may the rs2395471 variant relate to Long COVID or ME/CFS?

CD4+ T cell depletion and exhaustion are associated with COVID-19 severity and may reflect impaired adaptive immunity in Long COVID.

Can a consumer DNA test detect the rs2395471 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 rs2395471 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 CD4 and its variants. This is not an exhaustive literature review.

  • [1]PMID: 34316049
  • [2]Nature Genetics
  • [3]Journal of Clinical Investigation