{{Rsnum
|rsid=2305764
|Gene=MYO9B
|Chromosome=19
|position=17203024
|Orientation=minus
|GMAF=0.4146
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=MYO9B
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 39.8 | 44.2 | 15.9
| HCB | 4.5 | 38.8 | 56.7
| JPT | 9.7 | 27.4 | 62.8
| YRI | 10.2 | 42.9 | 46.9
| ASW | 17.9 | 41.1 | 41.1
| CHB | 4.5 | 38.8 | 56.7
| CHD | 8.3 | 33.0 | 58.7
| GIH | 13.9 | 58.4 | 27.7
| LWK | 11.0 | 56.0 | 33.0
| MEX | 6.9 | 48.3 | 44.8
| MKK | 7.7 | 46.8 | 45.5
| TSI | 33.3 | 52.9 | 13.7
| HapMapRevision=28
}}

[[rs2305764]] is a SNP in the untranslated region of the [[MYO9B]] gene that has been associated with [[celiac disease]], and thus [[gluten intolerance]]. The risk allele is [[rs2305764(T)]] as named in accordance with dbSNP. {{PMID|16282976}}

{{omim
|desc=CELIAC DISEASE, SUSCEPTIBILITY TO, 4; CELIAC4
|id=609753
|rsnum=2305764
}}

{{omim
|id=602129
|desc=MYOSIN IXB; MYO9B
|rsnum=2305764
}}

{{PMID Auto
|PMID=20096742
|Title=Intestinal barrier gene variants may not explain the increased levels of antigliadin antibodies, suggesting other mechanisms than altered permeability
}}

{{omim
|id=602129
|rsnum=2305764
|variant=0001
}}

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

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

{{PMID Auto
|PMID=17667713
|Title=Analysis of candidate genes on chromosomes 5q and 19p in celiac disease.
}}

{{PMID Auto
|PMID=17944996
|Title=The association of MYO9B gene in Italian patients with inflammatory bowel diseases.
}}

{{PMID Auto
|PMID=18361936
|Title=Association of MYO9B haplotype with type 1 diabetes.
}}

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

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

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

{{PMID Auto
|PMID=22954106
|Title=Myo9B is associated with an increased risk of Barrett's esophagus and esophageal adenocarcinoma.
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}