Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7517847
rs7517847
0.880 GeneticVariation BEFREE A significantly increased risk of CD early onset was observed in Poles carrying at least one rs7517847: G allele. 31052515

2019

dbSNP: rs7517847
rs7517847
0.880 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007

2016

dbSNP: rs7517847
rs7517847
0.880 GeneticVariation BEFREE Overall, a significant association was found between all CD and the rs7517847 polymorphism (OR = 0.699, 95% CI = 0.659 ~ 0.741, P < 0.001). 26678098

2015

dbSNP: rs7517847
rs7517847
0.880 GeneticVariation BEFREE OR = 1.409, 95% CI 1.279, 1.552).In conclusion, this meta-analysis demonstrates that rs7517847 is associated with the risk of CD in Caucasians. 26090488

2015

dbSNP: rs7517847
rs7517847
A 0.880 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919

2015

dbSNP: rs7517847
rs7517847
0.880 GeneticVariation BEFREE Rs1884444 was found to confer risk for UC and psoriasis, rs10889677 for CD and psoriasis, while rs2201841 and rs7517847 had effect only in CD. 23093364

2013

dbSNP: rs7517847
rs7517847
0.880 GeneticVariation BEFREE The present study confirms the association of the heterozygous and homozygous IL23R rs7517847 variant with CD and suggests an additive effect of smoking to the ATG16L1 rs2241879 C risk allele SNP, in the context of the multifactorial model established for the development of CD and a protective effect of the same allele against extra-intestinal manifestations. 21206965

2011

dbSNP: rs7517847
rs7517847
0.880 GeneticVariation BEFREE The rs7517847 variant, in contrast, was associated neither with CD nor with UC. 20192940

2010

dbSNP: rs7517847
rs7517847
0.880 GeneticVariation BEFREE Our meta-analysis supports that two polymorphisms (Arg381Gln and rs7517847) within the IL-23R gene may be considered to be protective factors against developing CD. 20157760

2010

dbSNP: rs7517847
rs7517847
0.880 GeneticVariation BEFREE The data show an association of both IL23R SNPs with overall IBD (statistically stronger, rs7517847; odds ratio [OR] = 0.79, 95% confidence interval [CI]: 0.67-0.94, minor allele frequencies: 0.355 in IBD patients versus 0.410 in controls; P = 0.005), somewhat stronger in Crohn's disease (OR = 0.74, 95% CI: 0.61-0.91) than in ulcerative colitis (OR = 0.84, 95% CI: 0.69-1.03). 18383521

2008

dbSNP: rs7517847
rs7517847
0.880 GeneticVariation GWASDB Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. 17435756

2007

dbSNP: rs7517847
rs7517847
0.880 GeneticVariation GWASCAT Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. 17435756

2007