rs1884613
Variant in the HNF4A gene (Hepatocyte Nuclear Factor 4 Alpha)
rs1884613 is a single nucleotide polymorphism (SNP) in the HNF4A gene, involved in hepatic gene regulation / MODY1. 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 rs1884613 variant?
rs1884613 is a SNP (single nucleotide polymorphism) in the HNF4A (Hepatocyte Nuclear Factor 4 Alpha) gene. It belongs to the Metabolic category and is part of the Metabolic Regulation biological cluster. HNF4A is a nuclear receptor critical for hepatic lipid and glucose metabolism and pancreatic beta cell function; mutations cause MODY1.
Biological role and pathway
This variant sits within the HNF4A gene, which is involved in the hepatic gene regulation / MODY1 pathway. Genes within the Metabolic 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.
rs1884613 and Long COVID / ME-CFS research
HNF4A regulates many liver genes involved in inflammation; variants may affect liver metabolism and COVID-19-associated hepatic dysfunction relevant to Long COVID.
This information is based on published research and does not constitute medical advice. See references below.
Parent gene: HNF4A
rs1884613 is one of 2 known variants in the HNF4A gene. To understand the full biological context of this variant, explore the parent gene page.
View HNF4A gene page →Conditions studied in relation to rs1884613
Research into HNF4A variants including rs1884613 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 HNF4A and the rs1884613 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 HNF4A gene
The following variants in HNF4A are also studied in relation to chronic illness and may be analysed together for a more complete picture.
Frequently asked questions
What is the rs1884613 variant in the HNF4A gene?
rs1884613 is a single nucleotide polymorphism (SNP) located in the HNF4A (Hepatocyte Nuclear Factor 4 Alpha) gene, which is involved in hepatic gene regulation / MODY1. HNF4A is a nuclear receptor critical for hepatic lipid and glucose metabolism and pancreatic beta cell function; mutations cause MODY1.
How may the rs1884613 variant relate to Long COVID or ME/CFS?
HNF4A regulates many liver genes involved in inflammation; variants may affect liver metabolism and COVID-19-associated hepatic dysfunction relevant to Long COVID.
Can a consumer DNA test detect the rs1884613 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 rs1884613 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 ReportInformational and educational only · Not a diagnostic tool · GDPR compliant
References
The following publications were used in compiling the research context for HNF4A and its variants. This is not an exhaustive literature review.
- [1]PMID: 33153018
- [2]Nature Genetics
- [3]NEJM