rs4241160

Variant in the PYCARD gene (PYD and CARD Domain Containing (ASC))

rs4241160 is a single nucleotide polymorphism (SNP) in the PYCARD gene, involved in inflammasome assembly. 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 rs4241160 variant?

rs4241160 is a SNP (single nucleotide polymorphism) in the PYCARD (PYD and CARD Domain Containing (ASC)) gene. It belongs to the Innate Immunity category and is part of the Innate Immunity & Pattern Recognition biological cluster. PYCARD encodes ASC, the inflammasome adaptor protein that bridges sensor proteins like NLRP3 to pro-caspase-1 for activation.

Biological role and pathway

This variant sits within the PYCARD gene, which is involved in the inflammasome assembly pathway. Genes within the Innate Immunity & Pattern Recognition 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.

rs4241160 and Long COVID / ME-CFS research

ASC-dependent inflammasome assembly is a key driver of IL-1beta and IL-18 release; variants may influence inflammatory severity in Long COVID.

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

Parent gene: PYCARD

rs4241160 is one of 1 known variant in the PYCARD gene. To understand the full biological context of this variant, explore the parent gene page.

View PYCARD gene page →

Conditions studied in relation to rs4241160

Research into PYCARD variants including rs4241160 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 PYCARD and the rs4241160 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 rs4241160 variant in the PYCARD gene?

rs4241160 is a single nucleotide polymorphism (SNP) located in the PYCARD (PYD and CARD Domain Containing (ASC)) gene, which is involved in inflammasome assembly. PYCARD encodes ASC, the inflammasome adaptor protein that bridges sensor proteins like NLRP3 to pro-caspase-1 for activation.

How may the rs4241160 variant relate to Long COVID or ME/CFS?

ASC-dependent inflammasome assembly is a key driver of IL-1beta and IL-18 release; variants may influence inflammatory severity in Long COVID.

Can a consumer DNA test detect the rs4241160 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 rs4241160 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 PYCARD and its variants. This is not an exhaustive literature review.

  • [1]PMID: 34088393
  • [2]Nature Genetics
  • [3]Journal of Clinical Investigation