SCN9A Gene
Sodium Voltage-Gated Channel Alpha Subunit 9 (SCN9A) is a gene involved in voltage-gated sodium channel signaling that has been studied in relation to immune function, metabolism, and chronic illness. Variants in SCN9A 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 SCN9A gene?
SCN9A encodes sodium voltage-gated channel alpha subunit 9, a protein involved in voltage-gated sodium channel signaling. It belongs to the Pain Sensory category and is part of the Pain & Sensory Processing biological cluster. SCN9A encodes Nav1.7, a voltage-gated sodium channel critical for pain signal transmission in peripheral sensory neurons.
Biological role and pathway
SCN9A is involved in the voltage-gated sodium channel signaling pathway, which plays a central role in regulating physiological processes relevant to immune defence, cellular energy, and systemic homeostasis. Genes within the Pain & Sensory Processing 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.
SCN9A and Long COVID / ME-CFS research
SCN9A variants affecting Nav1.7 function have been studied in relation to small fiber neuropathy and chronic pain in Long COVID.
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 SCN9A gene have been studied in relation to pain sensory and chronic illness. Each variant represents a single nucleotide position where individuals may carry different alleles.
Conditions studied in relation to SCN9A
Research into SCN9A variants has explored associations with the following conditions. These are areas of scientific investigation and do not imply that SCN9A 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 SCN9A and related genes in the pain & sensory processing 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 Pain & Sensory Processing pathway
SCN9A 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 SCN9A gene and what does it do?
SCN9A (Sodium Voltage-Gated Channel Alpha Subunit 9) is involved in voltage-gated sodium channel signaling. SCN9A encodes Nav1.7, a voltage-gated sodium channel critical for pain signal transmission in peripheral sensory neurons.
How may SCN9A gene variants relate to Long COVID or ME/CFS?
SCN9A variants affecting Nav1.7 function have been studied in relation to small fiber neuropathy and chronic pain in Long COVID.
Can a DNA test reveal information about my SCN9A 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 SCN9A 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.
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References
The following publications were used in compiling the research context for SCN9A. This is not an exhaustive literature review.
- [1]PMID: 32272069
- [2]Nature Genetics
- [3]Journal of Clinical Investigation