Gene entry
MAOA
monoamine oxidase A
- Chromosome
- X
- Cytoband
- Xp11.3
- Variants (rsID)
- 26
MAOA is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xp11.3). Its official name is “monoamine oxidase A”. The reference table lists 26 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs1137070Benignsingle nucleotide variantHistory of neurodevelopmental disorder|Brunner syndrome
- rs1800464Benignsingle nucleotide variantHistory of neurodevelopmental disorder|Brunner syndrome
- rs58524323Benignsingle nucleotide variantBrunner syndrome|History of neurodevelopmental disorder
- rs6323Benignsingle nucleotide variantHistory of neurodevelopmental disorder|Brunner syndrome
- rs138703731Conflicting interpretationssingle nucleotide variantBrunner syndrome|History of neurodevelopmental disorder
- rs1800466Conflicting interpretationssingle nucleotide variant
- rs72554632Pathogenicsingle nucleotide variantBrunner syndrome
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.