rs1883965
Variant in the MTOR gene (Mechanistic Target of Rapamycin Kinase)
rs1883965 is a single nucleotide polymorphism (SNP) in the MTOR gene, involved in mTOR 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 rs1883965 variant?
rs1883965 is a SNP (single nucleotide polymorphism) in the MTOR (Mechanistic Target of Rapamycin Kinase) gene. It belongs to the Signaling category and is part of the Cellular Signaling biological cluster. MTOR encodes the serine/threonine kinase that integrates nutrient, energy, and growth factor signals to regulate cell growth and autophagy.
Biological role and pathway
This variant sits within the MTOR gene, which is involved in the mTOR signaling pathway. Genes within the Cellular Signaling 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.
rs1883965 and Long COVID / ME-CFS research
mTOR pathway dysregulation has been studied in relation to immune activation, metabolic reprogramming, and impaired autophagy in Long COVID.
This information is based on published research and does not constitute medical advice. See references below.
Parent gene: MTOR
rs1883965 is one of 2 known variants in the MTOR gene. To understand the full biological context of this variant, explore the parent gene page.
View MTOR gene page →Conditions studied in relation to rs1883965
Research into MTOR variants including rs1883965 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 MTOR and the rs1883965 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 MTOR gene
The following variants in MTOR are also studied in relation to chronic illness and may be analysed together for a more complete picture.
Frequently asked questions
What is the rs1883965 variant in the MTOR gene?
rs1883965 is a single nucleotide polymorphism (SNP) located in the MTOR (Mechanistic Target of Rapamycin Kinase) gene, which is involved in mTOR signaling. MTOR encodes the serine/threonine kinase that integrates nutrient, energy, and growth factor signals to regulate cell growth and autophagy.
How may the rs1883965 variant relate to Long COVID or ME/CFS?
mTOR pathway dysregulation has been studied in relation to immune activation, metabolic reprogramming, and impaired autophagy in Long COVID.
Can a consumer DNA test detect the rs1883965 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 rs1883965 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 MTOR and its variants. This is not an exhaustive literature review.
- [1]PMID: 34316049
- [2]Nature Genetics
- [3]Journal of Clinical Investigation