{{Rsnum
|rsid=2006996
|Chromosome=9
|position=114830358
|Orientation=plus
|GMAF=0.141
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 8.0 | 92.0
| HCB | 13.1 | 41.6 | 45.3
| JPT | 26.5 | 46.9 | 26.5
| YRI | 0.0 | 6.1 | 93.9
| ASW | 0.0 | 7.0 | 93.0
| CHB | 13.1 | 41.6 | 45.3
| CHD | 7.3 | 42.2 | 50.5
| GIH | 2.0 | 17.8 | 80.2
| LWK | 0.9 | 13.6 | 85.5
| MEX | 1.7 | 32.8 | 65.5
| MKK | 0.0 | 11.5 | 88.5
| TSI | 0.0 | 2.0 | 98.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21699788
|Trait=None
|Title=HLA-Cw*1202-B*5201-DRB1*1502 Haplotype Increases Risk for Ulcerative Colitis But Reduces Risk for Crohn's Disease.
|RiskAllele=T
|Pval=4E-13
|OR=1.6700
|ORtxt=[1.47-1.92]
}}

{{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}}