rs61330082
Variant in the NAMPT gene (Nicotinamide Phosphoribosyltransferase)
rs61330082 is a single nucleotide polymorphism (SNP) in the NAMPT gene, involved in NAD+ biosynthesis / sirtuin activation. 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 rs61330082 variant?
rs61330082 is a SNP (single nucleotide polymorphism) in the NAMPT (Nicotinamide Phosphoribosyltransferase) gene. It belongs to the Metabolic category and is part of the Mitochondrial Energy Production & PEM biological cluster. NAMPT encodes the rate-limiting enzyme in the NAD+ salvage pathway, converting nicotinamide to NMN; also secreted as a pro-inflammatory cytokine (eNAMPT/PBEF).
Biological role and pathway
This variant sits within the NAMPT gene, which is involved in the NAD+ biosynthesis / sirtuin activation pathway. Genes within the Mitochondrial Energy Production & PEM 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.
rs61330082 and Long COVID / ME-CFS research
NAD+ depletion is implicated in Long COVID and ME/CFS fatigue; NAMPT variants affecting NAD+ biosynthesis may impair mitochondrial function and sirtuin activity in Long COVID.
This information is based on published research and does not constitute medical advice. See references below.
Parent gene: NAMPT
rs61330082 is one of 3 known variants in the NAMPT gene. To understand the full biological context of this variant, explore the parent gene page.
View NAMPT gene page →Conditions studied in relation to rs61330082
Research into NAMPT variants including rs61330082 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 NAMPT and the rs61330082 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 NAMPT gene
The following variants in NAMPT are also studied in relation to chronic illness and may be analysed together for a more complete picture.
Frequently asked questions
What is the rs61330082 variant in the NAMPT gene?
rs61330082 is a single nucleotide polymorphism (SNP) located in the NAMPT (Nicotinamide Phosphoribosyltransferase) gene, which is involved in NAD+ biosynthesis / sirtuin activation. NAMPT encodes the rate-limiting enzyme in the NAD+ salvage pathway, converting nicotinamide to NMN; also secreted as a pro-inflammatory cytokine (eNAMPT/PBEF).
How may the rs61330082 variant relate to Long COVID or ME/CFS?
NAD+ depletion is implicated in Long COVID and ME/CFS fatigue; NAMPT variants affecting NAD+ biosynthesis may impair mitochondrial function and sirtuin activity in Long COVID.
Can a consumer DNA test detect the rs61330082 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 rs61330082 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 NAMPT and its variants. This is not an exhaustive literature review.
- [1]PMID: 34316049
- [2]Cell
- [3]Nature Aging