{{Rsnum
|rsid=2371685
|Chromosome=5
|position=40392124
|Orientation=plus
|GMAF=0.1097
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 72.3 | 21.5 | 6.2
| HCB | 99.3 | 0.7 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 61.8 | 31.9 | 6.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 99.3 | 0.7 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 74.2 | 23.2 | 2.6
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{Report GE
|PubMed=17447842
|Source=pubmed
|AffyProbeset=SNP_A-4264860
|AffyOrientation=same
|AlleleA=A
|AlleleB=T
|onGW5=1
|rsid=2371685
|ancestral=A
|RiskPopulation=EU
|RiskAllele=T
|CaseFreq=0.19
|ControlFreq=0.13
|OddsRatioHet=
|OddsRatioHom=
|OddsRatioAll=1.56
|Disease=Crohn's disease
|DiseaseSymbol=CD
|OA=1
}}

rs2371685 is in linkage disequilibrium with a polymorphism that increases susceptibility to Crohn's disease 1.56 times for carriers of the T allele {{PMID|17447842|OA=1
}}
{{ neighbor
| rsid = 4613763
| distance = 502
}}

{{PMID Auto
|PMID=17903294
|Title=Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Affy500k}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}