{{Rsnum
|rsid=9267911
|Chromosome=6
|position=32237333
|Orientation=plus
|GMAF=0.416
|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 | 12.4 | 46.0 | 41.6
| HCB | 20.0 | 44.4 | 35.6
| JPT | 28.6 | 44.6 | 26.8
| YRI | 11.8 | 43.1 | 45.1
| ASW | 14.0 | 57.9 | 28.1
| CHB | 20.0 | 44.4 | 35.6
| CHD | 17.6 | 48.1 | 34.3
| GIH | 31.0 | 53.0 | 16.0
| LWK | 14.7 | 44.0 | 41.3
| MEX | 20.7 | 48.3 | 31.0
| MKK | 20.6 | 49.7 | 29.7
| TSI | 31.7 | 47.5 | 20.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23266558
  |Trait=Crohn's disease
  |Title=A Genome-Wide Association Study Identifies 2 Susceptibility Loci for Crohn's Disease in a Japanese Population.
  |RiskAllele=T
  |Pval=3E-7
  |OR=1.50
  |ORtxt=[1.29-1.76]
  }}

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