Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs917997
rs917997 		0.830 GeneticVariation BEFREE This meta-analysis provides robust estimates that IL18RAP rs917997 and CCR3 rs6441961 are potential risk factors for celiac disease in European populations. 26289103

2015
dbSNP: rs917997
rs917997 		0.830 GeneticVariation BEFREE Prior reports link rs917997 allele A with protection from T1D, and conversely with susceptibility to Celiac disease. 23891168

2013
dbSNP: rs917997
rs917997 		A 0.830 GeneticVariation GWASCAT Multiple common variants for celiac disease influencing immune gene expression. 20190752

2010
dbSNP: rs917997
rs917997 		A 0.830 GeneticVariation GWASDB Multiple common variants for celiac disease influencing immune gene expression. 20190752

2010
dbSNP: rs917997
rs917997 		0.830 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