{{Rsnum
|rsid=1736148
|Chromosome=21
|position=15440893
|Orientation=plus
|GMAF=0.3926
|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 | 18.8 | 47.3 | 33.9
| HCB | 4.4 | 28.5 | 67.2
| JPT | 2.7 | 29.2 | 68.1
| YRI | 36.3 | 46.6 | 17.1
| ASW | 25.0 | 53.6 | 21.4
| CHB | 4.4 | 28.5 | 67.2
| CHD | 5.6 | 28.7 | 65.7
| GIH | 8.9 | 41.6 | 49.5
| LWK | 33.9 | 52.3 | 13.8
| MEX | 24.1 | 50.0 | 25.9
| MKK | 33.3 | 53.8 | 12.8
| TSI | 15.0 | 45.0 | 40.0
| HapMapRevision=28
}}DeCode reports that [[rs1736148]] is associated with susceptibility to [[Crohn's disease]]. {{PMID|18587394|OA=1
}}

{{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}}