rs1800853

Variant in the POLG gene (DNA Polymerase Gamma Catalytic Subunit)

rs1800853 is a single nucleotide polymorphism (SNP) in the POLG gene, involved in mitochondrial DNA replication. 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 rs1800853 variant?

rs1800853 is a SNP (single nucleotide polymorphism) in the POLG (DNA Polymerase Gamma Catalytic Subunit) gene. It belongs to the Mitochondrial category and is part of the Mitochondrial Energy Production & PEM biological cluster. POLG encodes the catalytic subunit of mitochondrial DNA polymerase, essential for replication and repair of mitochondrial DNA.

Biological role and pathway

This variant sits within the POLG gene, which is involved in the mitochondrial DNA replication pathway. Genes within the Mitochondrial Energy Production & PEM 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.

rs1800853 and Long COVID / ME-CFS research

POLG variants affecting mitochondrial DNA integrity may compound mitochondrial dysfunction and fatigue associated with Long COVID.

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

Parent gene: POLG

rs1800853 is one of 2 known variants in the POLG gene. To understand the full biological context of this variant, explore the parent gene page.

View POLG gene page →

Conditions studied in relation to rs1800853

Research into POLG variants including rs1800853 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 POLG and the rs1800853 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 POLG gene

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

Frequently asked questions

What is the rs1800853 variant in the POLG gene?

rs1800853 is a single nucleotide polymorphism (SNP) located in the POLG (DNA Polymerase Gamma Catalytic Subunit) gene, which is involved in mitochondrial DNA replication. POLG encodes the catalytic subunit of mitochondrial DNA polymerase, essential for replication and repair of mitochondrial DNA.

How may the rs1800853 variant relate to Long COVID or ME/CFS?

POLG variants affecting mitochondrial DNA integrity may compound mitochondrial dysfunction and fatigue associated with Long COVID.

Can a consumer DNA test detect the rs1800853 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 rs1800853 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 POLG and its variants. This is not an exhaustive literature review.

  • [1]PMID: 32735956
  • [2]Nature Genetics
  • [3]Journal of Clinical Investigation