rs1047303

Variant in the HSD3B1 gene (Hydroxy-Delta-5-Steroid Dehydrogenase 3 Beta And Steroid Delta-Isomerase 1)

rs1047303 is a single nucleotide polymorphism (SNP) in the HSD3B1 gene, involved in adrenal steroid 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 rs1047303 variant?

rs1047303 is a SNP (single nucleotide polymorphism) in the HSD3B1 (Hydroxy-Delta-5-Steroid Dehydrogenase 3 Beta And Steroid Delta-Isomerase 1) gene. It belongs to the Hormonal category and is part of the Hormonal Regulation biological cluster. HSD3B1 encodes an enzyme essential for adrenal and gonadal steroid synthesis, converting pregnenolone to progesterone.

Biological role and pathway

This variant sits within the HSD3B1 gene, which is involved in the adrenal steroid 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.

rs1047303 and Long COVID / ME-CFS research

HSD3B1 variants affecting adrenal steroid production may contribute to adrenal insufficiency features reported in some Long COVID patients.

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

Parent gene: HSD3B1

rs1047303 is one of 1 known variant in the HSD3B1 gene. To understand the full biological context of this variant, explore the parent gene page.

View HSD3B1 gene page →

Conditions studied in relation to rs1047303

Research into HSD3B1 variants including rs1047303 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 HSD3B1 and the rs1047303 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 rs1047303 variant in the HSD3B1 gene?

rs1047303 is a single nucleotide polymorphism (SNP) located in the HSD3B1 (Hydroxy-Delta-5-Steroid Dehydrogenase 3 Beta And Steroid Delta-Isomerase 1) gene, which is involved in adrenal steroid synthesis. HSD3B1 encodes an enzyme essential for adrenal and gonadal steroid synthesis, converting pregnenolone to progesterone.

How may the rs1047303 variant relate to Long COVID or ME/CFS?

HSD3B1 variants affecting adrenal steroid production may contribute to adrenal insufficiency features reported in some Long COVID patients.

Can a consumer DNA test detect the rs1047303 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 rs1047303 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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Informational and educational only · Not a diagnostic tool · GDPR compliant

References

The following publications were used in compiling the research context for HSD3B1 and its variants. This is not an exhaustive literature review.

  • [1]PMID: 32972995
  • [2]Nature Genetics
  • [3]Journal of Clinical Investigation