rs1799836

What is the rs1799836 variant?

rs1799836 is a SNP (single nucleotide polymorphism) in the MAOB (Monoamine Oxidase B) gene. It belongs to the Neurotransmitter category and is part of the Methylation & Neurotransmitters biological cluster. MAOB encodes monoamine oxidase B, which preferentially catabolizes dopamine, benzylamine, and phenylethylamine.

Biological role and pathway

This variant sits within the MAOB gene, which is involved in the monoamine catabolism pathway. Genes within the Methylation & Neurotransmitters 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: MAOB

rs1799836 is one of 1 known variant in the MAOB gene. To understand the full biological context of this variant, explore the parent gene page.

Conditions studied in relation to rs1799836

Research into MAOB variants including rs1799836 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 MAOB and the rs1799836 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