rs3757441
Variant in the EZH2 gene (Enhancer Of Zeste 2 Polycomb Repressive Complex 2 Subunit)
rs3757441 is a single nucleotide polymorphism (SNP) in the EZH2 gene, involved in histone H3K27 methylation / gene silencing. 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 rs3757441 variant?
rs3757441 is a SNP (single nucleotide polymorphism) in the EZH2 (Enhancer Of Zeste 2 Polycomb Repressive Complex 2 Subunit) gene. It belongs to the Epigenetics category and is part of the Methylation & Neurotransmitters biological cluster. EZH2 is the catalytic subunit of PRC2 that trimethylates H3K27 for Polycomb-mediated gene silencing.
Biological role and pathway
This variant sits within the EZH2 gene, which is involved in the histone H3K27 methylation / gene silencing pathway. Genes within the Methylation & Neurotransmitters 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.
rs3757441 and Long COVID / ME-CFS research
EZH2-mediated H3K27me3 silencing regulates immune cell differentiation and antiviral gene expression; variants may affect epigenetic gene silencing and immune function in Long COVID.
This information is based on published research and does not constitute medical advice. See references below.
Parent gene: EZH2
rs3757441 is one of 1 known variant in the EZH2 gene. To understand the full biological context of this variant, explore the parent gene page.
View EZH2 gene page →Conditions studied in relation to rs3757441
Research into EZH2 variants including rs3757441 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 EZH2 and the rs3757441 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 rs3757441 variant in the EZH2 gene?
rs3757441 is a single nucleotide polymorphism (SNP) located in the EZH2 (Enhancer Of Zeste 2 Polycomb Repressive Complex 2 Subunit) gene, which is involved in histone H3K27 methylation / gene silencing. EZH2 is the catalytic subunit of PRC2 that trimethylates H3K27 for Polycomb-mediated gene silencing.
How may the rs3757441 variant relate to Long COVID or ME/CFS?
EZH2-mediated H3K27me3 silencing regulates immune cell differentiation and antiviral gene expression; variants may affect epigenetic gene silencing and immune function in Long COVID.
Can a consumer DNA test detect the rs3757441 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 rs3757441 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.
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References
The following publications were used in compiling the research context for EZH2 and its variants. This is not an exhaustive literature review.
- [1]PMID: 33664986
- [2]Nature Genetics
- [3]Cell