SCN3B Gene
Sodium Voltage-Gated Channel Beta Subunit 3 (SCN3B) is a gene involved in cardiac sodium channel modulation that has been studied in relation to immune function, metabolism, and chronic illness. Variants in SCN3B 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 SCN3B gene?
SCN3B encodes sodium voltage-gated channel beta subunit 3, a protein involved in cardiac sodium channel modulation. It belongs to the Cardiovascular category and is part of the Autonomic Nervous System biological cluster. SCN3B encodes the Nav beta-3 subunit that modulates SCN5A (Nav1.5) channel gating; mutations are linked to Brugada syndrome.
Biological role and pathway
SCN3B is involved in the cardiac sodium channel modulation pathway, which plays a central role in regulating physiological processes relevant to immune defence, cellular energy, and systemic homeostasis. Genes within the Autonomic Nervous System 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.
SCN3B and Long COVID / ME-CFS research
SCN3B modulates cardiac sodium channel function; variants may contribute to cardiac conduction abnormalities reported 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 SCN3B gene have been studied in relation to cardiovascular and chronic illness. Each variant represents a single nucleotide position where individuals may carry different alleles.
- rs13280585— SCN3B variant
Conditions studied in relation to SCN3B
Research into SCN3B variants has explored associations with the following conditions. These are areas of scientific investigation and do not imply that SCN3B 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 SCN3B and related genes in the autonomic nervous system 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 Autonomic Nervous System pathway
SCN3B 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 SCN3B gene and what does it do?
SCN3B (Sodium Voltage-Gated Channel Beta Subunit 3) is involved in cardiac sodium channel modulation. SCN3B encodes the Nav beta-3 subunit that modulates SCN5A (Nav1.5) channel gating; mutations are linked to Brugada syndrome.
How may SCN3B gene variants relate to Long COVID or ME/CFS?
SCN3B modulates cardiac sodium channel function; variants may contribute to cardiac conduction abnormalities reported in Long COVID.
Can a DNA test reveal information about my SCN3B 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 SCN3B 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 SCN3B. This is not an exhaustive literature review.
- [1]PMID: 32966261
- [2]Nature Genetics
- [3]Circulation