rs229069
Variant in the ADAMTS5 gene (ADAM Metallopeptidase With Thrombospondin Type 1 Motif 5)
rs229069 is a single nucleotide polymorphism (SNP) in the ADAMTS5 gene, involved in aggrecanase / cartilage remodeling. 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 rs229069 variant?
rs229069 is a SNP (single nucleotide polymorphism) in the ADAMTS5 (ADAM Metallopeptidase With Thrombospondin Type 1 Motif 5) gene. It belongs to the Connective Tissue category and is part of the Coagulation & Microcirculation biological cluster. ADAMTS5 is the primary aggrecanase that degrades aggrecan in cartilage, contributing to joint destruction.
Biological role and pathway
This variant sits within the ADAMTS5 gene, which is involved in the aggrecanase / cartilage remodeling 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.
rs229069 and Long COVID / ME-CFS research
ADAMTS5-mediated aggrecan degradation contributes to joint inflammation; variants may affect cartilage susceptibility to inflammatory joint damage in Long COVID.
This information is based on published research and does not constitute medical advice. See references below.
Parent gene: ADAMTS5
rs229069 is one of 1 known variant in the ADAMTS5 gene. To understand the full biological context of this variant, explore the parent gene page.
View ADAMTS5 gene page →Conditions studied in relation to rs229069
Research into ADAMTS5 variants including rs229069 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 ADAMTS5 and the rs229069 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 rs229069 variant in the ADAMTS5 gene?
rs229069 is a single nucleotide polymorphism (SNP) located in the ADAMTS5 (ADAM Metallopeptidase With Thrombospondin Type 1 Motif 5) gene, which is involved in aggrecanase / cartilage remodeling. ADAMTS5 is the primary aggrecanase that degrades aggrecan in cartilage, contributing to joint destruction.
How may the rs229069 variant relate to Long COVID or ME/CFS?
ADAMTS5-mediated aggrecan degradation contributes to joint inflammation; variants may affect cartilage susceptibility to inflammatory joint damage in Long COVID.
Can a consumer DNA test detect the rs229069 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 rs229069 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 ReportInformational and educational only · Not a diagnostic tool · GDPR compliant
References
The following publications were used in compiling the research context for ADAMTS5 and its variants. This is not an exhaustive literature review.
- [1]PMID: 33141942
- [2]Nature Genetics
- [3]Annals of the Rheumatic Diseases