rs703842

Variant in the CYP27B1 gene (Cytochrome P450 Family 27 Subfamily B Member 1)

rs703842 is a single nucleotide polymorphism (SNP) in the CYP27B1 gene, involved in vitamin D activation. 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 rs703842 variant?

rs703842 is a SNP (single nucleotide polymorphism) in the CYP27B1 (Cytochrome P450 Family 27 Subfamily B Member 1) gene. It belongs to the Vitamin Metabolism category and is part of the Vitamin & Nutrient Metabolism biological cluster. CYP27B1 encodes 1-alpha hydroxylase, the enzyme that converts 25-hydroxyvitamin D to the active form 1,25-dihydroxyvitamin D3.

Biological role and pathway

This variant sits within the CYP27B1 gene, which is involved in the vitamin D activation pathway. Genes within the Vitamin & Nutrient Metabolism 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.

rs703842 and Long COVID / ME-CFS research

CYP27B1 variants reducing vitamin D activation may impair immune regulation and increase susceptibility to persistent inflammation in Long COVID.

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

Parent gene: CYP27B1

rs703842 is one of 2 known variants in the CYP27B1 gene. To understand the full biological context of this variant, explore the parent gene page.

View CYP27B1 gene page →

Conditions studied in relation to rs703842

Research into CYP27B1 variants including rs703842 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 CYP27B1 and the rs703842 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 CYP27B1 gene

The following variants in CYP27B1 are also studied in relation to chronic illness and may be analysed together for a more complete picture.

Frequently asked questions

What is the rs703842 variant in the CYP27B1 gene?

rs703842 is a single nucleotide polymorphism (SNP) located in the CYP27B1 (Cytochrome P450 Family 27 Subfamily B Member 1) gene, which is involved in vitamin D activation. CYP27B1 encodes 1-alpha hydroxylase, the enzyme that converts 25-hydroxyvitamin D to the active form 1,25-dihydroxyvitamin D3.

How may the rs703842 variant relate to Long COVID or ME/CFS?

CYP27B1 variants reducing vitamin D activation may impair immune regulation and increase susceptibility to persistent inflammation in Long COVID.

Can a consumer DNA test detect the rs703842 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 rs703842 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 CYP27B1 and its variants. This is not an exhaustive literature review.

  • [1]PMID: 33153018
  • [2]Nature Genetics
  • [3]Journal of Clinical Investigation