{{Rsnum
|rsid=13015714
|Chromosome=2
|position=102355405
|Orientation=plus
|GMAF=0.2695
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=IL18R1
|Gene_s=IL18R1
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 3.5 | 33.6 | 62.8
| HCB | 21.9 | 48.9 | 29.2
| JPT | 8.0 | 57.5 | 34.5
| YRI | 1.4 | 17.7 | 81.0
| ASW | 0.0 | 14.0 | 86.0
| CHB | 21.9 | 48.9 | 29.2
| CHD | 24.8 | 55.0 | 20.2
| GIH | 18.8 | 48.5 | 32.7
| LWK | 0.0 | 19.1 | 80.9
| MEX | 15.5 | 58.6 | 25.9
| MKK | 1.9 | 19.2 | 78.8
| TSI | 5.9 | 29.4 | 64.7
| HapMapRevision=28
}}

{{GWAS Summary
|SNP=rs13015714
|PubMedID=18311140
|Condition=Celiac disease
|Gene=IL1RL1,IL18R1,IL18RAP, SLC9A4
|Risk Allele=C
|pValue=4.00E-009
|OR=1.28
|95CI=1.18-1.39
|OA=1
}}

{{omim
|desc=CELIAC DISEASE, SUSCEPTIBILITY TO, 8; CELIAC8
|id=612006
|rsnum=13015714
}}
{{PMID Auto
|PMID=19693089
|Title=Four novel coeliac disease regions replicated in an association study of a Swedish-Norwegian family cohort
}}

{{PharmGKB
|RSID=rs13015714
|Name_s=
|Gene_s=IL18R1
|Feature=
|Evidence=PubMed ID:18311140; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS Results: Newly identified genetic risk variants for celiac disease related to the immune response (Initial Sample Size: 767 cases, 1,422 controls; Replication Sample Size: 1,643 cases, 3,406 controls; Risk Allele: rs13015714-C).
|Drugs=
|Drug Classes=
|Diseases=Celiac Disease
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA162356752
}}

{{PMID Auto
|PMID=18853133
|Title=Gene variants influencing measures of inflammation or predisposing to autoimmune and inflammatory diseases are not associated with the risk of type 2 diabetes.
|OA=1
}}

{{PMID Auto
|PMID=19103669
|Title=Association study of the IL18RAP locus in three European populations with coeliac disease.
}}

{{PMID Auto
|PMID=19468064
|Title=Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs13015714
|overall_frequency_n=101
|overall_frequency_d=120
|overall_frequency=0.841667
|n_genomes=50
|n_genomes_annotated=0
|n_haplomes=86
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

{{PMID Auto GWAS
  |PMID=23042114
  |Trait=Atopic dermatitis
  |Title=Genome-wide association study identifies eight new susceptibility loci for atopic dermatitis in the Japanese population.
  |RiskAllele=G
  |Pval=8E-18
  |OR=1.27
  |ORtxt=[1.20-1.34]
  }}

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