rs41279104
Variant in the NOS1 gene (Nitric Oxide Synthase 1 (Neuronal))
rs41279104 is a single nucleotide polymorphism (SNP) in the NOS1 gene, involved in nitric oxide 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 rs41279104 variant?
rs41279104 is a SNP (single nucleotide polymorphism) in the NOS1 (Nitric Oxide Synthase 1 (Neuronal)) gene. It belongs to the Neurotransmitter category and is part of the Autonomic Nervous System biological cluster. NOS1 encodes neuronal NOS (nNOS), which produces nitric oxide in neurons to regulate synaptic transmission and vasodilation.
Biological role and pathway
This variant sits within the NOS1 gene, which is involved in the nitric oxide signaling pathway. Genes within the Autonomic Nervous System 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.
rs41279104 and Long COVID / ME-CFS research
NOS1 variants may affect neuronal nitric oxide signaling and contribute to cognitive and autonomic symptoms in Long COVID.
This information is based on published research and does not constitute medical advice. See references below.
Parent gene: NOS1
rs41279104 is one of 2 known variants in the NOS1 gene. To understand the full biological context of this variant, explore the parent gene page.
View NOS1 gene page →Conditions studied in relation to rs41279104
Research into NOS1 variants including rs41279104 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 NOS1 and the rs41279104 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 NOS1 gene
The following variants in NOS1 are also studied in relation to chronic illness and may be analysed together for a more complete picture.
Frequently asked questions
What is the rs41279104 variant in the NOS1 gene?
rs41279104 is a single nucleotide polymorphism (SNP) located in the NOS1 (Nitric Oxide Synthase 1 (Neuronal)) gene, which is involved in nitric oxide signaling. NOS1 encodes neuronal NOS (nNOS), which produces nitric oxide in neurons to regulate synaptic transmission and vasodilation.
How may the rs41279104 variant relate to Long COVID or ME/CFS?
NOS1 variants may affect neuronal nitric oxide signaling and contribute to cognitive and autonomic symptoms in Long COVID.
Can a consumer DNA test detect the rs41279104 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 rs41279104 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 NOS1 and its variants. This is not an exhaustive literature review.
- [1]PMID: 32272069
- [2]Nature Genetics
- [3]Journal of Clinical Investigation