{{Rsnum
|rsid=2927488
|Chromosome=19
|position=44728212
|Orientation=plus
|GMAF=0.2231
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 8.0 | 33.6 | 58.4
| HCB | 2.9 | 27.0 | 70.1
| JPT | 2.7 | 17.1 | 80.2
| YRI | 8.2 | 27.9 | 63.9
| ASW | 1.8 | 26.3 | 71.9
| CHB | 2.9 | 27.0 | 70.1
| CHD | 1.8 | 30.3 | 67.9
| GIH | 9.0 | 36.0 | 55.0
| LWK | 12.8 | 31.2 | 56.0
| MEX | 3.4 | 36.2 | 60.3
| MKK | 15.6 | 46.8 | 37.7
| TSI | 12.7 | 47.1 | 40.2
| HapMapRevision=28
}}{{PMID Auto
|PMID=20601676
|Title=Analysis of SNPs with an effect on gene expression identifies UBE2L3 and BCL3 as potential new risk genes for Crohn's disease
}}

{{PMID Auto
|PMID=21390209
|Title=Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease.
|OA=1
}}

{{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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}