{{Rsnum
|rsid=1457092
|Gene=MYO9B
|Chromosome=19
|position=17193427
|Orientation=minus
|GMAF=0.4568
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=MYO9B
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 42.2 | 42.2 | 15.6
| HCB | 2.2 | 35.6 | 62.2
| JPT | 11.4 | 34.1 | 54.5
| YRI | 14.3 | 47.6 | 38.1
| ASW | 0.0 | 0.0 | 0.0
| CHB | 2.2 | 35.6 | 62.2
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=20096742
|Title=Intestinal barrier gene variants may not explain the increased levels of antigliadin antibodies, suggesting other mechanisms than altered permeability
}}

{{PMID|17176439}} No evidence of association of the MYO9B polymorphisms with celiac disease in the Spanish population.

{{PMID|17584584}} MYO9B gene polymorphisms are associated with autoimmune diseases in Spanish population.

{{PMID|19142207|OA=1
}} MYO9B polymorphisms in multiple sclerosis.

{{PMID|20303373}} Association analysis of myosin IXB and type 1 diabetes.

{{PMID|21515326}} Replication of genetic variation in the MYO9B gene in Crohn's disease.

{{PMID Auto
|PMID=23368647
|Title=Frequency of MYO9B polymorphisms in celiac patients and controls
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}