{{Rsnum
|rsid=1799836
|Gene=MAOB
|Chromosome=X
|position=43768752
|Orientation=minus
|GMAF=0.4311
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=MAOB
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 49.1 | 22.3 | 28.6
| HCB | 68.4 | 22.8 | 8.8
| JPT | 76.8 | 16.1 | 7.1
| YRI | 14.3 | 15.0 | 70.7
| ASW | 19.3 | 22.8 | 57.9
| CHB | 68.4 | 22.8 | 8.8
| CHD | 72.4 | 16.2 | 11.4
| GIH | 57.4 | 12.9 | 29.7
| LWK | 13.6 | 15.5 | 70.9
| MEX | 53.4 | 31.0 | 15.5
| MKK | 16.7 | 20.5 | 62.8
| TSI | 45.5 | 21.8 | 32.7
| HapMapRevision=28
}}{{PMID|18205889}} [[Parkinson's disease]] The risk alleles for each SNP identified from conditional logistic regression, [[rs1721100]] C, [[rs1721082]] T and [[rs1799836]] A, are consistent with previous reports.
Significant interaction between this [[MAOB]] SNP and a [[FGF20]] SNP, [[rs1721100]] was also noticed.

{{PMID Auto
|PMID=19657584
|Title=Negative emotionality: monoamine oxidase B gene variants modulate personality traits in healthy humans
|OA=1
}}

{{PMID Auto
|PMID=21978760
|Title=Association study of monoamine oxidase A/B genes and schizophrenia in Han Chinese
|OA=1
}}

{{PMID Auto
|PMID=16174289
|Title=MAOA haplotypes associated with thrombocyte-MAO activity.
|OA=1
}}

{{PMID Auto
|PMID=16848906
|Title=Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans.
|OA=1
}}

{{PMID Auto
|PMID=17427196
|Title=Monoamine oxidase A gene polymorphism predicts adolescent outcome of attention-deficit/hyperactivity disorder.
}}

{{PMID Auto
|PMID=17918234
|Title=The monoamine oxidase B gene exhibits significant association to ADHD.
}}

{{PMID Auto
|PMID=18180394
|Title=Genetic variation within adrenergic pathways determines in vivo effects of presynaptic stimulation in humans.
|OA=1
}}

{{PMID Auto
|PMID=19018232
|Title=Comparison of the genotyping results using DNA obtained from blood and saliva.
|OA=1
}}

{{PMID Auto
|PMID=19344875
|Title=Association test for X-linked QTL in family-based designs.
|OA=1
}}

{{PMID Auto
|PMID=19772600
|Title=A comparison of classification methods for predicting Chronic Fatigue Syndrome based on genetic data.
|OA=1
}}

{{PMID Auto
|PMID=23111930
|Title=MAOA and MAOB polymorphisms and anger-related traits in suicidal participants and controls
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}