rs1880676

What is the rs1880676 variant?

rs1880676 is a SNP (single nucleotide polymorphism) in the CHAT (Choline O-Acetyltransferase) gene. It belongs to the Neurotransmitter category and is part of the Autonomic Nervous System biological cluster. CHAT encodes choline acetyltransferase, the enzyme that synthesizes acetylcholine from acetyl-CoA and choline in cholinergic neurons.

Biological role and pathway

This variant sits within the CHAT gene, which is involved in the acetylcholine biosynthesis pathway. Genes within the Autonomic Nervous System 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.

Parent gene: CHAT

rs1880676 is one of 1 known variant in the CHAT gene. To understand the full biological context of this variant, explore the parent gene page.

Conditions studied in relation to rs1880676

Research into CHAT variants including rs1880676 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 CHAT and the rs1880676 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