ADAMTS13 Gene
ADAM Metallopeptidase With Thrombospondin Type 1 Motif 13 (ADAMTS13) is a gene involved in VWF processing that has been studied in relation to immune function, metabolism, and chronic illness. Variants in ADAMTS13 may influence how the body responds to infection, inflammation, and long-term recovery.
This page is for educational and informational purposes only. Not a diagnostic tool. Always consult a qualified healthcare provider.
What is the ADAMTS13 gene?
ADAMTS13 encodes adam metallopeptidase with thrombospondin type 1 motif 13, a protein involved in VWF processing. It belongs to the Coagulation category and is part of the Coagulation & Vascular biological cluster. ADAMTS13 cleaves ultra-large VWF multimers released from endothelium into smaller, less adhesive forms. Deficiency causes thrombotic thrombocytopenic purpura (TTP) with widespread microvascular platelet thrombi.
Biological role and pathway
ADAMTS13 is involved in the VWF processing pathway, which plays a central role in regulating physiological processes relevant to immune defence, cellular energy, and systemic homeostasis. Genes within the Coagulation & Vascular 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 in these systems — particularly under conditions of physiological stress such as viral infection or prolonged illness.
ADAMTS13 and Long COVID / ME-CFS research
ADAMTS13 deficiency relative to elevated VWF is documented in severe COVID-19 and Long COVID, creating TTP-like microangiopathy. ADAMTS13 variants affecting VWF processing capacity may predispose to widespread microthrombi characteristic of Long COVID vascular disease.
This information is based on published research and does not constitute medical advice. See references below.
Known genetic variants
The following variants (SNPs) in the ADAMTS13 gene have been studied in relation to coagulation and chronic illness. Each variant represents a single nucleotide position where individuals may carry different alleles.
- rs2285489— ADAMTS13 variant
- rs1048659— ADAMTS13 variant
- rs28933409— ADAMTS13 variant
Conditions studied in relation to ADAMTS13
Research into ADAMTS13 variants has explored associations with the following conditions. These are areas of scientific investigation and do not imply that ADAMTS13 causes or treats any condition.
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 ADAMTS13 and related genes in the coagulation & vascular pathway.
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.
Related genes in the Coagulation & Vascular pathway
ADAMTS13 does not act in isolation. The following genes are functionally related and may be analysed together for a more complete picture of your genetic predispositions.
Frequently asked questions
What is the ADAMTS13 gene and what does it do?
ADAMTS13 (ADAM Metallopeptidase With Thrombospondin Type 1 Motif 13) is involved in VWF processing. ADAMTS13 cleaves ultra-large VWF multimers released from endothelium into smaller, less adhesive forms. Deficiency causes thrombotic thrombocytopenic purpura (TTP) with widespread microvascular platelet thrombi.
How may ADAMTS13 gene variants relate to Long COVID or ME/CFS?
ADAMTS13 deficiency relative to elevated VWF is documented in severe COVID-19 and Long COVID, creating TTP-like microangiopathy. ADAMTS13 variants affecting VWF processing capacity may predispose to widespread microthrombi characteristic of Long COVID vascular disease.
Can a DNA test reveal information about my ADAMTS13 gene?
Consumer DNA data from 23andMe, AncestryDNA, and MyHeritage includes SNP variants for many genes. ChronicDNA analyses your raw DNA file and reports on variants that have been studied in relation to chronic illness, immune function, and metabolism. This is not a diagnostic service — results are informational and educational only.
Explore your ADAMTS13 genetic insights
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 ADAMTS13. This is not an exhaustive literature review.
- [1]PMID: 32826326
- [2]Blood
- [3]New England Journal of Medicine