rs1549596

Variant in the ISG15 gene (ISG15 Ubiquitin Like Modifier)

rs1549596 is a single nucleotide polymorphism (SNP) in the ISG15 gene, involved in ISGylation antiviral defense. 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 rs1549596 variant?

rs1549596 is a SNP (single nucleotide polymorphism) in the ISG15 (ISG15 Ubiquitin Like Modifier) gene. It belongs to the Antiviral category and is part of the Viral Defense & Interferon Response biological cluster. ISG15 encodes an interferon-stimulated ubiquitin-like modifier that conjugates to viral and host proteins, restricting viral replication.

Biological role and pathway

This variant sits within the ISG15 gene, which is involved in the ISGylation antiviral defense pathway. Genes within the Viral Defense & Interferon Response 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.

rs1549596 and Long COVID / ME-CFS research

ISG15 is a key antiviral ISGylation factor; deficiency causes type I interferonopathy, while variants may influence Long COVID susceptibility through altered interferon signaling.

This information is based on published research and does not constitute medical advice. See references below.

Parent gene: ISG15

rs1549596 is one of 1 known variant in the ISG15 gene. To understand the full biological context of this variant, explore the parent gene page.

View ISG15 gene page →

Conditions studied in relation to rs1549596

Research into ISG15 variants including rs1549596 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 ISG15 and the rs1549596 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 rs1549596 variant in the ISG15 gene?

rs1549596 is a single nucleotide polymorphism (SNP) located in the ISG15 (ISG15 Ubiquitin Like Modifier) gene, which is involved in ISGylation antiviral defense. ISG15 encodes an interferon-stimulated ubiquitin-like modifier that conjugates to viral and host proteins, restricting viral replication.

How may the rs1549596 variant relate to Long COVID or ME/CFS?

ISG15 is a key antiviral ISGylation factor; deficiency causes type I interferonopathy, while variants may influence Long COVID susceptibility through altered interferon signaling.

Can a consumer DNA test detect the rs1549596 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 rs1549596 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 Report

Informational and educational only · Not a diagnostic tool · GDPR compliant

References

The following publications were used in compiling the research context for ISG15 and its variants. This is not an exhaustive literature review.

  • [1]PMID: 32217835
  • [2]Nature Immunology
  • [3]NEJM