rs66766036

Variant in the AR gene (Androgen Receptor)

rs66766036 is a single nucleotide polymorphism (SNP) in the AR gene, involved in androgen signaling. 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 rs66766036 variant?

rs66766036 is a SNP (single nucleotide polymorphism) in the AR (Androgen Receptor) gene. It belongs to the Hormonal category and is part of the Hormonal Regulation biological cluster. AR encodes the androgen receptor, which mediates testosterone and DHT effects on immune function, muscle, and metabolism.

Biological role and pathway

This variant sits within the AR gene, which is involved in the androgen signaling pathway. Genes within the Hormonal Regulation 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.

rs66766036 and Long COVID / ME-CFS research

AR variants may influence sex-specific immune responses and testosterone-mediated immune modulation relevant to Long COVID sex differences.

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

Parent gene: AR

rs66766036 is one of 2 known variants in the AR gene. To understand the full biological context of this variant, explore the parent gene page.

View AR gene page →

Conditions studied in relation to rs66766036

Research into AR variants including rs66766036 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 AR and the rs66766036 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.

Other variants in the AR gene

The following variants in AR are also studied in relation to chronic illness and may be analysed together for a more complete picture.

Frequently asked questions

What is the rs66766036 variant in the AR gene?

rs66766036 is a single nucleotide polymorphism (SNP) located in the AR (Androgen Receptor) gene, which is involved in androgen signaling. AR encodes the androgen receptor, which mediates testosterone and DHT effects on immune function, muscle, and metabolism.

How may the rs66766036 variant relate to Long COVID or ME/CFS?

AR variants may influence sex-specific immune responses and testosterone-mediated immune modulation relevant to Long COVID sex differences.

Can a consumer DNA test detect the rs66766036 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 rs66766036 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 AR and its variants. This is not an exhaustive literature review.

  • [1]PMID: 34316049
  • [2]Nature Genetics
  • [3]Journal of Clinical Investigation