PROS1 Gene
Protein S1 (PROS1) is a gene involved in anticoagulation that has been studied in relation to immune function, metabolism, and chronic illness. Variants in PROS1 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 PROS1 gene?
PROS1 encodes protein s1, a protein involved in anticoagulation. It belongs to the Coagulation category and is part of the Coagulation & Vascular biological cluster. Protein S is the vitamin K-dependent cofactor for activated protein C (APC). Free protein S enhances APC inactivation of factors Va and VIIIa and independently inhibits factor Xa; deficiency causes recurrent venous thromboembolism.
Biological role and pathway
PROS1 is involved in the anticoagulation 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.
PROS1 and Long COVID / ME-CFS research
Free protein S levels are reduced in COVID-19 due to acute phase increases in C4b-binding protein. Protein S deficiency with PROS1 variants may compound COVID-19-associated hypercoagulability, increasing risk of Long COVID vascular thrombosis.
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 PROS1 gene have been studied in relation to coagulation and chronic illness. Each variant represents a single nucleotide position where individuals may carry different alleles.
- rs7590268— PROS1 variant
- rs15904— PROS1 variant
- rs79452681— PROS1 variant
Conditions studied in relation to PROS1
Research into PROS1 variants has explored associations with the following conditions. These are areas of scientific investigation and do not imply that PROS1 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 PROS1 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
PROS1 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 PROS1 gene and what does it do?
PROS1 (Protein S1) is involved in anticoagulation. Protein S is the vitamin K-dependent cofactor for activated protein C (APC). Free protein S enhances APC inactivation of factors Va and VIIIa and independently inhibits factor Xa; deficiency causes recurrent venous thromboembolism.
How may PROS1 gene variants relate to Long COVID or ME/CFS?
Free protein S levels are reduced in COVID-19 due to acute phase increases in C4b-binding protein. Protein S deficiency with PROS1 variants may compound COVID-19-associated hypercoagulability, increasing risk of Long COVID vascular thrombosis.
Can a DNA test reveal information about my PROS1 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 PROS1 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 PROS1. This is not an exhaustive literature review.
- [1]PMID: 29728449
- [2]Blood
- [3]Thrombosis and Haemostasis