rs2074058
Variant in the FFAR3 gene (Free Fatty Acid Receptor 3)
rs2074058 is a single nucleotide polymorphism (SNP) in the FFAR3 gene, involved in SCFA 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 rs2074058 variant?
rs2074058 is a SNP (single nucleotide polymorphism) in the FFAR3 (Free Fatty Acid Receptor 3) gene. It belongs to the Gut Microbiome category and is part of the Gut-Brain Axis biological cluster. FFAR3 (GPR41) responds primarily to propionate and butyrate and is expressed in enteroendocrine cells and the sympathetic nervous system, connecting gut microbial metabolism to autonomic regulation.
Biological role and pathway
This variant sits within the FFAR3 gene, which is involved in the SCFA signaling pathway. Genes within the Gut-Brain Axis 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.
rs2074058 and Long COVID / ME-CFS research
FFAR3-mediated signaling links gut SCFA production to autonomic nervous system tone. In POTS and dysautonomia associated with Long COVID, impaired FFAR3 signaling from dysbiotic gut may contribute to sympathetic-parasympathetic imbalance.
This information is based on published research and does not constitute medical advice. See references below.
Parent gene: FFAR3
rs2074058 is one of 2 known variants in the FFAR3 gene. To understand the full biological context of this variant, explore the parent gene page.
View FFAR3 gene page →Conditions studied in relation to rs2074058
Research into FFAR3 variants including rs2074058 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 FFAR3 and the rs2074058 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 FFAR3 gene
The following variants in FFAR3 are also studied in relation to chronic illness and may be analysed together for a more complete picture.
Frequently asked questions
What is the rs2074058 variant in the FFAR3 gene?
rs2074058 is a single nucleotide polymorphism (SNP) located in the FFAR3 (Free Fatty Acid Receptor 3) gene, which is involved in SCFA signaling. FFAR3 (GPR41) responds primarily to propionate and butyrate and is expressed in enteroendocrine cells and the sympathetic nervous system, connecting gut microbial metabolism to autonomic regulation.
How may the rs2074058 variant relate to Long COVID or ME/CFS?
FFAR3-mediated signaling links gut SCFA production to autonomic nervous system tone. In POTS and dysautonomia associated with Long COVID, impaired FFAR3 signaling from dysbiotic gut may contribute to sympathetic-parasympathetic imbalance.
Can a consumer DNA test detect the rs2074058 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.
Related articles
- Long COVID Dysautonomia: What Your Genes May Reveal
Explore how genes in the autonomic nervous system may relate to Long COVID dysautonomia, including POTS, heart rate changes and orthostatic intolerance.
- Long COVID POTS: Symptoms, Testing and Genetics
Learn how Long COVID POTS affects heart rate, how standing and tilt table tests assess it, and which genes research is exploring.
Find out if you carry the rs2074058 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 FFAR3 and its variants. This is not an exhaustive literature review.
- [1]PMID: 28167838
- [2]Nature Neuroscience
- [3]Cell Metabolism