SCN1A Gene

Sodium Voltage-Gated Channel Alpha Subunit 1 (SCN1A) is a gene involved in neuronal sodium channel / excitability that has been studied in relation to immune function, metabolism, and chronic illness. Variants in SCN1A 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 SCN1A gene?

SCN1A encodes sodium voltage-gated channel alpha subunit 1, a protein involved in neuronal sodium channel / excitability. It belongs to the Neurological category and is part of the Neurological & Cognitive Function biological cluster. SCN1A encodes Nav1.1, the primary neuronal sodium channel in inhibitory interneurons; loss-of-function causes Dravet syndrome.

Biological role and pathway

SCN1A is involved in the neuronal sodium channel / excitability 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.

SCN1A and Long COVID / ME-CFS research

SCN1A variants affecting inhibitory interneuron function may contribute to neurological hyperexcitability and sensory sensitization in Long COVID neurological presentations.

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 SCN1A gene have been studied in relation to neurological and chronic illness. Each variant represents a single nucleotide position where individuals may carry different alleles.

Conditions studied in relation to SCN1A

Research into SCN1A variants has explored associations with the following conditions. These are areas of scientific investigation and do not imply that SCN1A causes or treats any condition.

Long CovidNeurologicalSensory Sensitivity

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 SCN1A 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

SCN1A 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 SCN1A gene and what does it do?

SCN1A (Sodium Voltage-Gated Channel Alpha Subunit 1) is involved in neuronal sodium channel / excitability. SCN1A encodes Nav1.1, the primary neuronal sodium channel in inhibitory interneurons; loss-of-function causes Dravet syndrome.

How may SCN1A gene variants relate to Long COVID or ME/CFS?

SCN1A variants affecting inhibitory interneuron function may contribute to neurological hyperexcitability and sensory sensitization in Long COVID neurological presentations.

Can a DNA test reveal information about my SCN1A 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 SCN1A 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 Report

Informational and educational only · Not a diagnostic tool · GDPR compliant

References

The following publications were used in compiling the research context for SCN1A. This is not an exhaustive literature review.

  • [1]PMID: 33664986
  • [2]Nature Genetics
  • [3]Nature Neuroscience