rs248793
Variant in the SRD5A1 gene (Steroid 5 Alpha-Reductase 1)
rs248793 is a single nucleotide polymorphism (SNP) in the SRD5A1 gene, involved in DHT 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 rs248793 variant?
rs248793 is a SNP (single nucleotide polymorphism) in the SRD5A1 (Steroid 5 Alpha-Reductase 1) gene. It belongs to the Hormonal category and is part of the Hormonal Regulation biological cluster. SRD5A1 encodes steroid 5-alpha reductase type 1, which converts testosterone to the more potent androgen dihydrotestosterone.
Biological role and pathway
This variant sits within the SRD5A1 gene, which is involved in the DHT synthesis 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.
rs248793 and Long COVID / ME-CFS research
SRD5A1 variants may modulate androgen levels and sex-specific immune regulation relevant to Long COVID sex differences.
This information is based on published research and does not constitute medical advice. See references below.
Parent gene: SRD5A1
rs248793 is one of 1 known variant in the SRD5A1 gene. To understand the full biological context of this variant, explore the parent gene page.
View SRD5A1 gene page →Conditions studied in relation to rs248793
Research into SRD5A1 variants including rs248793 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 SRD5A1 and the rs248793 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 rs248793 variant in the SRD5A1 gene?
rs248793 is a single nucleotide polymorphism (SNP) located in the SRD5A1 (Steroid 5 Alpha-Reductase 1) gene, which is involved in DHT synthesis. SRD5A1 encodes steroid 5-alpha reductase type 1, which converts testosterone to the more potent androgen dihydrotestosterone.
How may the rs248793 variant relate to Long COVID or ME/CFS?
SRD5A1 variants may modulate androgen levels and sex-specific immune regulation relevant to Long COVID sex differences.
Can a consumer DNA test detect the rs248793 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 rs248793 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.
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References
The following publications were used in compiling the research context for SRD5A1 and its variants. This is not an exhaustive literature review.
- [1]PMID: 34316049
- [2]Nature Genetics
- [3]Journal of Clinical Investigation