rs2279343

Variant in the CYP2B6 gene (Cytochrome P450 Family 2 Subfamily B Member 6)

rs2279343 is a single nucleotide polymorphism (SNP) in the CYP2B6 gene, involved in Phase I xenobiotic metabolism. 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 rs2279343 variant?

rs2279343 is a SNP (single nucleotide polymorphism) in the CYP2B6 (Cytochrome P450 Family 2 Subfamily B Member 6) gene. It belongs to the Drug Metabolism category and is part of the Detox & Medication Sensitivity biological cluster. CYP2B6 encodes a hepatic cytochrome P450 enzyme involved in metabolizing bupropion, efavirenz, and many other drugs.

Biological role and pathway

This variant sits within the CYP2B6 gene, which is involved in the Phase I xenobiotic metabolism pathway. Genes within the Detox & Medication Sensitivity 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.

rs2279343 and Long COVID / ME-CFS research

CYP2B6 variants affect metabolism of medications including antidepressants and antivirals that may be used in Long COVID management.

This information is based on published research and does not constitute medical advice. See references below.

Parent gene: CYP2B6

rs2279343 is one of 2 known variants in the CYP2B6 gene. To understand the full biological context of this variant, explore the parent gene page.

View CYP2B6 gene page →

Conditions studied in relation to rs2279343

Research into CYP2B6 variants including rs2279343 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 CYP2B6 and the rs2279343 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.

Other variants in the CYP2B6 gene

The following variants in CYP2B6 are also studied in relation to chronic illness and may be analysed together for a more complete picture.

Frequently asked questions

What is the rs2279343 variant in the CYP2B6 gene?

rs2279343 is a single nucleotide polymorphism (SNP) located in the CYP2B6 (Cytochrome P450 Family 2 Subfamily B Member 6) gene, which is involved in Phase I xenobiotic metabolism. CYP2B6 encodes a hepatic cytochrome P450 enzyme involved in metabolizing bupropion, efavirenz, and many other drugs.

How may the rs2279343 variant relate to Long COVID or ME/CFS?

CYP2B6 variants affect metabolism of medications including antidepressants and antivirals that may be used in Long COVID management.

Can a consumer DNA test detect the rs2279343 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 rs2279343 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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Informational and educational only · Not a diagnostic tool · GDPR compliant

References

The following publications were used in compiling the research context for CYP2B6 and its variants. This is not an exhaustive literature review.

  • [1]PMID: 26014458
  • [2]Nature Genetics
  • [3]Journal of Clinical Investigation