rs36012910

Variant in the DNMT3A gene (DNA Methyltransferase 3 Alpha)

rs36012910 is a single nucleotide polymorphism (SNP) in the DNMT3A gene, involved in de novo DNA methylation. 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 rs36012910 variant?

rs36012910 is a SNP (single nucleotide polymorphism) in the DNMT3A (DNA Methyltransferase 3 Alpha) gene. It belongs to the Epigenetics category and is part of the Epigenetics & Gene Regulation biological cluster. DNMT3A encodes a de novo DNA methyltransferase that establishes new methylation patterns on CpG sites during development and in response to environmental signals.

Biological role and pathway

This variant sits within the DNMT3A gene, which is involved in the de novo DNA methylation pathway. Genes within the Epigenetics & Gene Regulation 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.

rs36012910 and Long COVID / ME-CFS research

Epigenetic reprogramming via DNMT3A may alter immune gene expression patterns contributing to persistent immune dysregulation in Long COVID.

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

Parent gene: DNMT3A

rs36012910 is one of 2 known variants in the DNMT3A gene. To understand the full biological context of this variant, explore the parent gene page.

View DNMT3A gene page →

Conditions studied in relation to rs36012910

Research into DNMT3A variants including rs36012910 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 DNMT3A and the rs36012910 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 DNMT3A gene

The following variants in DNMT3A are also studied in relation to chronic illness and may be analysed together for a more complete picture.

Frequently asked questions

What is the rs36012910 variant in the DNMT3A gene?

rs36012910 is a single nucleotide polymorphism (SNP) located in the DNMT3A (DNA Methyltransferase 3 Alpha) gene, which is involved in de novo DNA methylation. DNMT3A encodes a de novo DNA methyltransferase that establishes new methylation patterns on CpG sites during development and in response to environmental signals.

How may the rs36012910 variant relate to Long COVID or ME/CFS?

Epigenetic reprogramming via DNMT3A may alter immune gene expression patterns contributing to persistent immune dysregulation in Long COVID.

Can a consumer DNA test detect the rs36012910 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 rs36012910 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 DNMT3A and its variants. This is not an exhaustive literature review.

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