rs2301995
Variant in the ELN gene (Elastin)
rs2301995 is a single nucleotide polymorphism (SNP) in the ELN gene, involved in elastic fiber assembly / vascular compliance. 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 rs2301995 variant?
rs2301995 is a SNP (single nucleotide polymorphism) in the ELN (Elastin) gene. It belongs to the Connective Tissue category and is part of the Coagulation & Microcirculation biological cluster. ELN encodes elastin, the structural protein providing elasticity to arteries, lungs, skin, and other tissues.
Biological role and pathway
This variant sits within the ELN gene, which is involved in the elastic fiber assembly / vascular compliance 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.
rs2301995 and Long COVID / ME-CFS research
Elastin integrity is critical for vascular and lung compliance; ELN variants may affect vascular elasticity and contribute to dysautonomia or pulmonary complications in Long COVID.
This information is based on published research and does not constitute medical advice. See references below.
Parent gene: ELN
rs2301995 is one of 1 known variant in the ELN gene. To understand the full biological context of this variant, explore the parent gene page.
View ELN gene page →Conditions studied in relation to rs2301995
Research into ELN variants including rs2301995 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 ELN and the rs2301995 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 rs2301995 variant in the ELN gene?
rs2301995 is a single nucleotide polymorphism (SNP) located in the ELN (Elastin) gene, which is involved in elastic fiber assembly / vascular compliance. ELN encodes elastin, the structural protein providing elasticity to arteries, lungs, skin, and other tissues.
How may the rs2301995 variant relate to Long COVID or ME/CFS?
Elastin integrity is critical for vascular and lung compliance; ELN variants may affect vascular elasticity and contribute to dysautonomia or pulmonary complications in Long COVID.
Can a consumer DNA test detect the rs2301995 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 rs2301995 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 ELN and its variants. This is not an exhaustive literature review.
- [1]PMID: 32966261
- [2]Nature Genetics
- [3]Circulation