rs779805
Variant in the VHL gene (Von Hippel-Lindau Tumor Suppressor)
rs779805 is a single nucleotide polymorphism (SNP) in the VHL gene, involved in HIF-alpha ubiquitination / oxygen sensing. 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 rs779805 variant?
rs779805 is a SNP (single nucleotide polymorphism) in the VHL (Von Hippel-Lindau Tumor Suppressor) gene. It belongs to the Signaling category and is part of the Mitochondrial Energy Production & PEM biological cluster. VHL encodes the substrate recognition component of an E3 ubiquitin ligase that targets HIF-alpha for proteasomal degradation under normoxia.
Biological role and pathway
This variant sits within the VHL gene, which is involved in the HIF-alpha ubiquitination / oxygen sensing 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.
rs779805 and Long COVID / ME-CFS research
VHL-mediated HIF degradation is essential for normoxic regulation; variants affecting VHL function may alter baseline HIF activity and the hypoxic response in Long COVID.
This information is based on published research and does not constitute medical advice. See references below.
Parent gene: VHL
rs779805 is one of 1 known variant in the VHL gene. To understand the full biological context of this variant, explore the parent gene page.
View VHL gene page →Conditions studied in relation to rs779805
Research into VHL variants including rs779805 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 VHL and the rs779805 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.
Frequently asked questions
What is the rs779805 variant in the VHL gene?
rs779805 is a single nucleotide polymorphism (SNP) located in the VHL (Von Hippel-Lindau Tumor Suppressor) gene, which is involved in HIF-alpha ubiquitination / oxygen sensing. VHL encodes the substrate recognition component of an E3 ubiquitin ligase that targets HIF-alpha for proteasomal degradation under normoxia.
How may the rs779805 variant relate to Long COVID or ME/CFS?
VHL-mediated HIF degradation is essential for normoxic regulation; variants affecting VHL function may alter baseline HIF activity and the hypoxic response in Long COVID.
Can a consumer DNA test detect the rs779805 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 rs779805 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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References
The following publications were used in compiling the research context for VHL and its variants. This is not an exhaustive literature review.
- [1]PMID: 34316049
- [2]Nature Genetics
- [3]NEJM