rs6721961
Variant in the NRF2 gene (Nuclear Factor Erythroid 2-Like 2 (Nrf2))
rs6721961 is a single nucleotide polymorphism (SNP) in the NRF2 gene, involved in antioxidant response element 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 rs6721961 variant?
rs6721961 is a SNP (single nucleotide polymorphism) in the NRF2 (Nuclear Factor Erythroid 2-Like 2 (Nrf2)) gene. It belongs to the Oxidative Stress category and is part of the Oxidative Stress biological cluster. NRF2 is the master transcription factor activating antioxidant gene programs in response to oxidative and electrophilic stress.
Biological role and pathway
This variant sits within the NRF2 gene, which is involved in the antioxidant response element signaling pathway. Genes within the Oxidative Stress 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.
rs6721961 and Long COVID / ME-CFS research
Nrf2 pathway activation is a key cellular defense; variants may determine resilience to Long COVID oxidative and inflammatory stress.
This information is based on published research and does not constitute medical advice. See references below.
Parent gene: NRF2
rs6721961 is one of 2 known variants in the NRF2 gene. To understand the full biological context of this variant, explore the parent gene page.
View NRF2 gene page →Conditions studied in relation to rs6721961
Research into NRF2 variants including rs6721961 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 NRF2 and the rs6721961 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 NRF2 gene
The following variants in NRF2 are also studied in relation to chronic illness and may be analysed together for a more complete picture.
Frequently asked questions
What is the rs6721961 variant in the NRF2 gene?
rs6721961 is a single nucleotide polymorphism (SNP) located in the NRF2 (Nuclear Factor Erythroid 2-Like 2 (Nrf2)) gene, which is involved in antioxidant response element signaling. NRF2 is the master transcription factor activating antioxidant gene programs in response to oxidative and electrophilic stress.
How may the rs6721961 variant relate to Long COVID or ME/CFS?
Nrf2 pathway activation is a key cellular defense; variants may determine resilience to Long COVID oxidative and inflammatory stress.
Can a consumer DNA test detect the rs6721961 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 rs6721961 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 NRF2 and its variants. This is not an exhaustive literature review.
- [1]PMID: 34088393
- [2]Nature Genetics
- [3]Journal of Clinical Investigation