rs17883901
Variant in the GCLC gene (Glutamate-Cysteine Ligase Catalytic Subunit)
rs17883901 is a single nucleotide polymorphism (SNP) in the GCLC gene, involved in glutathione biosynthesis. 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 rs17883901 variant?
rs17883901 is a SNP (single nucleotide polymorphism) in the GCLC (Glutamate-Cysteine Ligase Catalytic Subunit) gene. It belongs to the Oxidative Stress category and is part of the Oxidative Stress biological cluster. GCLC encodes the catalytic subunit of glutamate-cysteine ligase, the rate-limiting enzyme in glutathione synthesis.
Biological role and pathway
This variant sits within the GCLC gene, which is involved in the glutathione biosynthesis 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.
rs17883901 and Long COVID / ME-CFS research
Glutathione depletion is a major feature of COVID-19 pathophysiology; GCLC variants may reduce antioxidant capacity and worsen Long COVID oxidative stress.
This information is based on published research and does not constitute medical advice. See references below.
Parent gene: GCLC
rs17883901 is one of 1 known variant in the GCLC gene. To understand the full biological context of this variant, explore the parent gene page.
View GCLC gene page →Conditions studied in relation to rs17883901
Research into GCLC variants including rs17883901 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 GCLC and the rs17883901 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 rs17883901 variant in the GCLC gene?
rs17883901 is a single nucleotide polymorphism (SNP) located in the GCLC (Glutamate-Cysteine Ligase Catalytic Subunit) gene, which is involved in glutathione biosynthesis. GCLC encodes the catalytic subunit of glutamate-cysteine ligase, the rate-limiting enzyme in glutathione synthesis.
How may the rs17883901 variant relate to Long COVID or ME/CFS?
Glutathione depletion is a major feature of COVID-19 pathophysiology; GCLC variants may reduce antioxidant capacity and worsen Long COVID oxidative stress.
Can a consumer DNA test detect the rs17883901 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 rs17883901 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 GCLC and its variants. This is not an exhaustive literature review.
- [1]PMID: 25122754
- [2]Nature Genetics
- [3]Journal of Clinical Investigation