Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1343151
rs1343151
0.010 GeneticVariation BEFREE In comparison to disease-matched controls, patients with CD developing psoriasis following IFX therapy were more likely to be homozygous for specific polymorphisms in the IL-23R gene (rs10489628, rs10789229, and rs1343151). 23274341

2013

dbSNP: rs2241880
rs2241880
0.010 GeneticVariation BEFREE T300A variant of autophagy ATG16L1 gene is associated with decreased antigen sampling and processing by dendritic cells in pediatric Crohn's disease. 24022642

2013

dbSNP: rs11209026
rs11209026
0.010 GeneticVariation BEFREE We confirmed the findings that the IL-23 receptor gene coding variant allele R381Q appears to decrease susceptibility to CD in an Israeli Jewish population. 18030204

2007

dbSNP: rs1248696
rs1248696
0.010 GeneticVariation BEFREE DLG5 R30Q variant is a female-specific protective factor in pediatric onset Crohn's disease. 17156146

2007

dbSNP: rs2165047
rs2165047
0.010 GeneticVariation BEFREE Polymorphisms 3020insC in CARD15 and SNP rs2165047 in DLG5 were associated with specific phenotypes in this pediatric-onset CD cohort. 17476680

2007

dbSNP: rs3792876
rs3792876
0.010 GeneticVariation BEFREE Polymorphisms 3020insC in CARD15 and SNP rs3792876 in SLC22A4/5 occurred statistically significantly more often in patients with pediatric-onset CD than in patients with adult-onset CD. 17476680

2007