rs281865436

Variant in the G6PC gene (Glucose-6-Phosphatase Catalytic Subunit)

rs281865436 is a single nucleotide polymorphism (SNP) in the G6PC gene, involved in hepatic glucose output / glycogen storage. 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 rs281865436 variant?

rs281865436 is a SNP (single nucleotide polymorphism) in the G6PC (Glucose-6-Phosphatase Catalytic Subunit) gene. It belongs to the Metabolic category and is part of the Metabolic Regulation biological cluster. G6PC encodes glucose-6-phosphatase, the liver enzyme catalyzing the final step in gluconeogenesis and glycogenolysis.

Biological role and pathway

This variant sits within the G6PC gene, which is involved in the hepatic glucose output / glycogen storage pathway. Genes within the Metabolic 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.

rs281865436 and Long COVID / ME-CFS research

G6PC variants affect hepatic glucose production; liver dysfunction in COVID-19 may impair G6PC-mediated glucose homeostasis, contributing to metabolic complications in Long COVID.

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

Parent gene: G6PC

rs281865436 is one of 1 known variant in the G6PC gene. To understand the full biological context of this variant, explore the parent gene page.

View G6PC gene page →

Conditions studied in relation to rs281865436

Research into G6PC variants including rs281865436 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 G6PC and the rs281865436 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 rs281865436 variant in the G6PC gene?

rs281865436 is a single nucleotide polymorphism (SNP) located in the G6PC (Glucose-6-Phosphatase Catalytic Subunit) gene, which is involved in hepatic glucose output / glycogen storage. G6PC encodes glucose-6-phosphatase, the liver enzyme catalyzing the final step in gluconeogenesis and glycogenolysis.

How may the rs281865436 variant relate to Long COVID or ME/CFS?

G6PC variants affect hepatic glucose production; liver dysfunction in COVID-19 may impair G6PC-mediated glucose homeostasis, contributing to metabolic complications in Long COVID.

Can a consumer DNA test detect the rs281865436 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 rs281865436 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 G6PC and its variants. This is not an exhaustive literature review.

  • [1]PMID: 33153018
  • [2]Nature Genetics
  • [3]Hepatology