rs2279697

Variant in the HADHA gene (Hydroxyacyl-CoA Dehydrogenase Trifunctional Multienzyme Complex Subunit Alpha)

rs2279697 is a single nucleotide polymorphism (SNP) in the HADHA gene, involved in mitochondrial fatty acid oxidation. 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 rs2279697 variant?

rs2279697 is a SNP (single nucleotide polymorphism) in the HADHA (Hydroxyacyl-CoA Dehydrogenase Trifunctional Multienzyme Complex Subunit Alpha) gene. It belongs to the Mitochondrial category and is part of the Mitochondrial Energy Production & PEM biological cluster. HADHA encodes three enzymatic activities of the mitochondrial trifunctional protein complex involved in fatty acid beta-oxidation.

Biological role and pathway

This variant sits within the HADHA gene, which is involved in the mitochondrial fatty acid oxidation pathway. Genes within the Mitochondrial Energy Production & PEM 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.

rs2279697 and Long COVID / ME-CFS research

HADHA function supports efficient mitochondrial fat oxidation; variants may impair energy metabolism in peripheral tissues affected by Long COVID.

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

Parent gene: HADHA

rs2279697 is one of 1 known variant in the HADHA gene. To understand the full biological context of this variant, explore the parent gene page.

View HADHA gene page →

Conditions studied in relation to rs2279697

Research into HADHA variants including rs2279697 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 HADHA and the rs2279697 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 HADHA gene

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

Frequently asked questions

What is the rs2279697 variant in the HADHA gene?

rs2279697 is a single nucleotide polymorphism (SNP) located in the HADHA (Hydroxyacyl-CoA Dehydrogenase Trifunctional Multienzyme Complex Subunit Alpha) gene, which is involved in mitochondrial fatty acid oxidation. HADHA encodes three enzymatic activities of the mitochondrial trifunctional protein complex involved in fatty acid beta-oxidation.

How may the rs2279697 variant relate to Long COVID or ME/CFS?

HADHA function supports efficient mitochondrial fat oxidation; variants may impair energy metabolism in peripheral tissues affected by Long COVID.

Can a consumer DNA test detect the rs2279697 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 rs2279697 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.

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 HADHA and its variants. This is not an exhaustive literature review.

  • [1]PMID: 32735956
  • [2]Nature Genetics
  • [3]Journal of Clinical Investigation