rs1293762
Variant in the OAS2 gene (2'-5'-Oligoadenylate Synthetase 2)
rs1293762 is a single nucleotide polymorphism (SNP) in the OAS2 gene, involved in innate antiviral defense. 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 rs1293762 variant?
rs1293762 is a SNP (single nucleotide polymorphism) in the OAS2 (2'-5'-Oligoadenylate Synthetase 2) gene. It belongs to the Antiviral category and is part of the Viral Defense & Interferon Response biological cluster. OAS2 encodes a medium-size OAS enzyme that contributes to the antiviral 2-5A/RNase L system.
Biological role and pathway
This variant sits within the OAS2 gene, which is involved in the innate antiviral defense pathway. Genes within the Viral Defense & Interferon Response 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.
rs1293762 and Long COVID / ME-CFS research
OAS2 variants may influence the robustness of innate antiviral responses to SARS-CoV-2, with implications for viral clearance and Long COVID risk.
This information is based on published research and does not constitute medical advice. See references below.
Parent gene: OAS2
rs1293762 is one of 1 known variant in the OAS2 gene. To understand the full biological context of this variant, explore the parent gene page.
View OAS2 gene page →Conditions studied in relation to rs1293762
Research into OAS2 variants including rs1293762 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 OAS2 and the rs1293762 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.
Frequently asked questions
What is the rs1293762 variant in the OAS2 gene?
rs1293762 is a single nucleotide polymorphism (SNP) located in the OAS2 (2'-5'-Oligoadenylate Synthetase 2) gene, which is involved in innate antiviral defense. OAS2 encodes a medium-size OAS enzyme that contributes to the antiviral 2-5A/RNase L system.
How may the rs1293762 variant relate to Long COVID or ME/CFS?
OAS2 variants may influence the robustness of innate antiviral responses to SARS-CoV-2, with implications for viral clearance and Long COVID risk.
Can a consumer DNA test detect the rs1293762 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 rs1293762 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 OAS2 and its variants. This is not an exhaustive literature review.
- [1]PMID: 34385711
- [2]Nature Genetics
- [3]Journal of Infectious Diseases