rs13015714, IL18R1

N. diseases: 3
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
0.810 GeneticVariation BEFREE In this study, two previously indicated risk variants at the IL18RAP locus (rs13015714 and rs917997) were tested for genetic association in 1638 cases with coeliac disease and 1385 control individuals from the Finnish, Hungarian and Italian populations. 19103669 2009
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
0.810 GeneticVariation GWASCAT Newly identified genetic risk variants for celiac disease related to the immune response. 18311140 2008
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
0.810 GeneticVariation GWASDB Newly identified genetic risk variants for celiac disease related to the immune response. 18311140 2008
Dermatitis, Atopic
CUI: C0011615
Disease: Dermatitis, Atopic
0.800 GeneticVariation GWASCAT Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis. 26482879 2015
Dermatitis, Atopic
CUI: C0011615
Disease: Dermatitis, Atopic
0.800 GeneticVariation GWASDB Genome-wide association study identifies eight new susceptibility loci for atopic dermatitis in the Japanese population. 23042114 2012
Dermatitis, Atopic
CUI: C0011615
Disease: Dermatitis, Atopic
0.800 GeneticVariation GWASCAT Genome-wide association study identifies eight new susceptibility loci for atopic dermatitis in the Japanese population. 23042114 2012
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
0.010 GeneticVariation BEFREE By combining homo- and heterozygous carriers of the rs13015714 risk allele, differences were still significant for both CD adult- and pediatric-onset. 23634226 2013