rs2232372
Variant in the HAS2 gene (Hyaluronan Synthase 2)
rs2232372 is a single nucleotide polymorphism (SNP) in the HAS2 gene, involved in hyaluronan synthesis. 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 rs2232372 variant?
rs2232372 is a SNP (single nucleotide polymorphism) in the HAS2 (Hyaluronan Synthase 2) gene. It belongs to the Connective Tissue category and is part of the Immune System & Inflammation biological cluster. HAS2 encodes hyaluronan synthase 2, which synthesizes high-molecular-weight hyaluronic acid.
Biological role and pathway
This variant sits within the HAS2 gene, which is involved in the hyaluronan synthesis pathway. Genes within the Immune System & Inflammation 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.
rs2232372 and Long COVID / ME-CFS research
COVID-19 promotes hyaluronic acid overproduction in the lung, causing hydrogel formation in alveoli; HAS2 variants may affect the severity of this pathology and related Long COVID pulmonary symptoms.
This information is based on published research and does not constitute medical advice. See references below.
Parent gene: HAS2
rs2232372 is one of 1 known variant in the HAS2 gene. To understand the full biological context of this variant, explore the parent gene page.
View HAS2 gene page →Conditions studied in relation to rs2232372
Research into HAS2 variants including rs2232372 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 HAS2 and the rs2232372 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 rs2232372 variant in the HAS2 gene?
rs2232372 is a single nucleotide polymorphism (SNP) located in the HAS2 (Hyaluronan Synthase 2) gene, which is involved in hyaluronan synthesis. HAS2 encodes hyaluronan synthase 2, which synthesizes high-molecular-weight hyaluronic acid.
How may the rs2232372 variant relate to Long COVID or ME/CFS?
COVID-19 promotes hyaluronic acid overproduction in the lung, causing hydrogel formation in alveoli; HAS2 variants may affect the severity of this pathology and related Long COVID pulmonary symptoms.
Can a consumer DNA test detect the rs2232372 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 rs2232372 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 HAS2 and its variants. This is not an exhaustive literature review.
- [1]PMID: 33141942
- [2]Matrix Biology
- [3]Nature Medicine