{{Rsnum
|rsid=7714584
|Chromosome=5
|position=150890858
|Orientation=plus
|GMAF=0.2828
|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 | 91.2 | 8.8 | 0.0
| HCB | 33.8 | 49.3 | 16.9
| JPT | 41.1 | 42.9 | 16.1
| YRI | 20.4 | 52.4 | 27.2
| ASW | 28.1 | 47.4 | 24.6
| CHB | 33.8 | 49.3 | 16.9
| CHD | 28.7 | 53.7 | 17.6
| GIH | 72.3 | 24.8 | 3.0
| LWK | 37.0 | 46.3 | 16.7
| MEX | 72.4 | 24.1 | 3.4
| MKK | 51.6 | 40.0 | 8.4
| TSI | 71.6 | 27.5 | 1.0
| HapMapRevision=28
}}[http://blog.23andme.com/2008/08/25/researchers-find-biological-basis-for-crohns-association/ 23andMe blog] [[rs7714584]](G) linked with an increased risk for [[Crohn's disease]]. Similar to [[rs13361189]]

{{PMID Auto GWAS
|PMID=21102463
|Trait=None
|Title=Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
|RiskAllele=G
|Pval=8E-19
|OR=1.3700
|ORtxt=[1.28-1.47]
|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}}