rs222747
Variant in the TRPV1 gene (Transient Receptor Potential Vanilloid 1)
rs222747 is a single nucleotide polymorphism (SNP) in the TRPV1 gene, involved in pain and sensory 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 rs222747 variant?
rs222747 is a SNP (single nucleotide polymorphism) in the TRPV1 (Transient Receptor Potential Vanilloid 1) gene. It belongs to the Pain Sensory category and is part of the Pain & Sensory Processing biological cluster. TRPV1 encodes a non-selective cation channel activated by heat, capsaicin, and pro-inflammatory mediators, central to pain transduction.
Biological role and pathway
This variant sits within the TRPV1 gene, which is involved in the pain and sensory signaling pathway. Genes within the Pain & Sensory Processing 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.
rs222747 and Long COVID / ME-CFS research
TRPV1 sensitization by inflammatory mediators may contribute to widespread pain, hyperalgesia, and sensory amplification in Long COVID.
This information is based on published research and does not constitute medical advice. See references below.
Parent gene: TRPV1
rs222747 is one of 2 known variants in the TRPV1 gene. To understand the full biological context of this variant, explore the parent gene page.
View TRPV1 gene page →Conditions studied in relation to rs222747
Research into TRPV1 variants including rs222747 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 TRPV1 and the rs222747 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 TRPV1 gene
The following variants in TRPV1 are also studied in relation to chronic illness and may be analysed together for a more complete picture.
Frequently asked questions
What is the rs222747 variant in the TRPV1 gene?
rs222747 is a single nucleotide polymorphism (SNP) located in the TRPV1 (Transient Receptor Potential Vanilloid 1) gene, which is involved in pain and sensory signaling. TRPV1 encodes a non-selective cation channel activated by heat, capsaicin, and pro-inflammatory mediators, central to pain transduction.
How may the rs222747 variant relate to Long COVID or ME/CFS?
TRPV1 sensitization by inflammatory mediators may contribute to widespread pain, hyperalgesia, and sensory amplification in Long COVID.
Can a consumer DNA test detect the rs222747 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 rs222747 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 TRPV1 and its variants. This is not an exhaustive literature review.
- [1]PMID: 32272069
- [2]Nature Genetics
- [3]Journal of Clinical Investigation