NEFL Gene
Neurofilament Light Chain (NEFL) is a gene involved in axon structural integrity / neurodegeneration biomarker that has been studied in relation to immune function, metabolism, and chronic illness. Variants in NEFL may influence how the body responds to infection, inflammation, and long-term recovery.
This page is for educational and informational purposes only. Not a diagnostic tool. Always consult a qualified healthcare provider.
What is the NEFL gene?
NEFL encodes neurofilament light chain, a protein involved in axon structural integrity / neurodegeneration biomarker. It belongs to the Neurological category and is part of the Neurological & Cognitive Function biological cluster. NEFL encodes neurofilament light chain, the most abundant neurofilament protein; serum NfL is a sensitive biomarker of axonal injury and neurodegeneration.
Biological role and pathway
NEFL is involved in the axon structural integrity / neurodegeneration biomarker pathway, which plays a central role in regulating physiological processes relevant to immune defence, cellular energy, and systemic homeostasis. Genes within the Neurological & Cognitive Function 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 in these systems — particularly under conditions of physiological stress such as viral infection or prolonged illness.
NEFL and Long COVID / ME-CFS research
Serum neurofilament light (NfL) is elevated in Long COVID patients with neurological symptoms, reflecting axonal damage; NEFL variants may affect neuronal fragility and Long COVID neurological outcomes.
This information is based on published research and does not constitute medical advice. See references below.
Known genetic variants
The following variants (SNPs) in the NEFL gene have been studied in relation to neurological and chronic illness. Each variant represents a single nucleotide position where individuals may carry different alleles.
- rs1805902— NEFL variant
Conditions studied in relation to NEFL
Research into NEFL variants has explored associations with the following conditions. These are areas of scientific investigation and do not imply that NEFL causes or treats any condition.
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 NEFL and related genes in the neurological & cognitive function pathway.
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.
Related genes in the Neurological & Cognitive Function pathway
NEFL does not act in isolation. The following genes are functionally related and may be analysed together for a more complete picture of your genetic predispositions.
Frequently asked questions
What is the NEFL gene and what does it do?
NEFL (Neurofilament Light Chain) is involved in axon structural integrity / neurodegeneration biomarker. NEFL encodes neurofilament light chain, the most abundant neurofilament protein; serum NfL is a sensitive biomarker of axonal injury and neurodegeneration.
How may NEFL gene variants relate to Long COVID or ME/CFS?
Serum neurofilament light (NfL) is elevated in Long COVID patients with neurological symptoms, reflecting axonal damage; NEFL variants may affect neuronal fragility and Long COVID neurological outcomes.
Can a DNA test reveal information about my NEFL gene?
Consumer DNA data from 23andMe, AncestryDNA, and MyHeritage includes SNP variants for many genes. ChronicDNA analyses your raw DNA file and reports on variants that have been studied in relation to chronic illness, immune function, and metabolism. This is not a diagnostic service — results are informational and educational only.
Explore your NEFL genetic insights
Upload your DNA data from 23andMe, AncestryDNA, or MyHeritage and receive a personalised report covering >80 genes relevant to Long COVID and ME/CFS.
Get Your Personalised DNA ReportInformational and educational only · Not a diagnostic tool · GDPR compliant
References
The following publications were used in compiling the research context for NEFL. This is not an exhaustive literature review.
- [1]PMID: 33664986
- [2]Nature Medicine
- [3]Cell