rs6453645

Variant in the VEGFB gene (Vascular Endothelial Growth Factor B)

rs6453645 is a single nucleotide polymorphism (SNP) in the VEGFB gene, involved in cardiac vascular growth. 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 rs6453645 variant?

rs6453645 is a SNP (single nucleotide polymorphism) in the VEGFB (Vascular Endothelial Growth Factor B) gene. It belongs to the Vascular category and is part of the Coagulation & Microcirculation biological cluster. VEGFB encodes a vascular growth factor that promotes cardiac muscle growth and fatty acid transport rather than angiogenesis.

Biological role and pathway

This variant sits within the VEGFB gene, which is involved in the cardiac vascular growth pathway. Genes within the Coagulation & Microcirculation 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.

rs6453645 and Long COVID / ME-CFS research

VEGFB may influence cardiac vascular regeneration and myocardial perfusion relevant to cardiac manifestations of Long COVID.

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

Parent gene: VEGFB

rs6453645 is one of 1 known variant in the VEGFB gene. To understand the full biological context of this variant, explore the parent gene page.

View VEGFB gene page →

Conditions studied in relation to rs6453645

Research into VEGFB variants including rs6453645 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 VEGFB and the rs6453645 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 rs6453645 variant in the VEGFB gene?

rs6453645 is a single nucleotide polymorphism (SNP) located in the VEGFB (Vascular Endothelial Growth Factor B) gene, which is involved in cardiac vascular growth. VEGFB encodes a vascular growth factor that promotes cardiac muscle growth and fatty acid transport rather than angiogenesis.

How may the rs6453645 variant relate to Long COVID or ME/CFS?

VEGFB may influence cardiac vascular regeneration and myocardial perfusion relevant to cardiac manifestations of Long COVID.

Can a consumer DNA test detect the rs6453645 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 rs6453645 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 VEGFB and its variants. This is not an exhaustive literature review.

  • [1]PMID: 32734001
  • [2]Nature Genetics
  • [3]Journal of Clinical Investigation