rs1741981
Variant in the HDAC1 gene (Histone Deacetylase 1)
rs1741981 is a single nucleotide polymorphism (SNP) in the HDAC1 gene, involved in histone deacetylation. 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 rs1741981 variant?
rs1741981 is a SNP (single nucleotide polymorphism) in the HDAC1 (Histone Deacetylase 1) gene. It belongs to the Epigenetics category and is part of the Epigenetics & Gene Regulation biological cluster. HDAC1 encodes a class I histone deacetylase that removes acetyl groups from histones, compacting chromatin and repressing transcription.
Biological role and pathway
This variant sits within the HDAC1 gene, which is involved in the histone deacetylation 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.
rs1741981 and Long COVID / ME-CFS research
HDAC1-mediated epigenetic regulation may modulate inflammatory gene expression patterns relevant to Long COVID immune dysregulation.
This information is based on published research and does not constitute medical advice. See references below.
Parent gene: HDAC1
rs1741981 is one of 1 known variant in the HDAC1 gene. To understand the full biological context of this variant, explore the parent gene page.
View HDAC1 gene page →Conditions studied in relation to rs1741981
Research into HDAC1 variants including rs1741981 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 HDAC1 and the rs1741981 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 HDAC1 gene
The following variants in HDAC1 are also studied in relation to chronic illness and may be analysed together for a more complete picture.
Frequently asked questions
What is the rs1741981 variant in the HDAC1 gene?
rs1741981 is a single nucleotide polymorphism (SNP) located in the HDAC1 (Histone Deacetylase 1) gene, which is involved in histone deacetylation. HDAC1 encodes a class I histone deacetylase that removes acetyl groups from histones, compacting chromatin and repressing transcription.
How may the rs1741981 variant relate to Long COVID or ME/CFS?
HDAC1-mediated epigenetic regulation may modulate inflammatory gene expression patterns relevant to Long COVID immune dysregulation.
Can a consumer DNA test detect the rs1741981 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 rs1741981 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 HDAC1 and its variants. This is not an exhaustive literature review.
- [1]PMID: 34316049
- [2]Nature Genetics
- [3]Journal of Clinical Investigation