{{Rsnum
|rsid=1373692
|Chromosome=5
|position=40431081
|Orientation=minus
|GMAF=0.4761
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 39.8 | 49.6 | 10.6
| HCB | 4.4 | 21.9 | 73.7
| JPT | 0.9 | 24.8 | 74.3
| YRI | 45.2 | 42.5 | 12.3
| ASW | 38.6 | 49.1 | 12.3
| CHB | 4.4 | 21.9 | 73.7
| CHD | 0.9 | 26.6 | 72.5
| GIH | 20.8 | 42.6 | 36.6
| LWK | 57.3 | 34.5 | 8.2
| MEX | 24.1 | 44.8 | 31.0
| MKK | 37.8 | 43.6 | 18.6
| TSI | 30.4 | 52.9 | 16.7
| HapMapRevision=28
}}

rs1373692 increases susceptibility to Crohn's disease 1.46 times for carriers of the G allele {{PMID|17447842|OA=1
}}

{{GWAS Summary
|SNP=rs1373692
|PubMedID=17447842
|Condition=Crohn's disease
|Gene=Intergenic
|Risk Allele=
|pValue=2.00E-012
|OR=1.46
|95CI=
|OA=1
}}

{{omim
|desc=INFLAMMATORY BOWEL DISEASE 18; IBD18
|id=612262
|rsnum=1373692
}}

{{PharmGKB
|RSID=rs1373692
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:17447842; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4 (Initial Sample Size: 547 cases, 928 controls; Replication Sample Size: 1,266 cases, 559 controls, 428 trios). This variant is associated with Crohn's disease.
|Drugs=
|Drug Classes=
|Diseases=Crohn Disease
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA162356567
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1373692
|overall_frequency_n=74
|overall_frequency_d=128
|overall_frequency=0.578125
|n_genomes=39
|n_genomes_annotated=0
|n_haplomes=60
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

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