Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1545620
rs1545620
0.060 GeneticVariation BEFREE This meta-analysis suggested that rs1545620 is both CD and UC susceptible locus in Caucasians; rs1457092 and rs2305764 are UC susceptible loci, but are not CD susceptible loci in Caucasians. 27435931

2016

dbSNP: rs1545620
rs1545620
0.060 GeneticVariation BEFREE Furthermore, stratification analyses indicated that rs1545620 decreased the risk of IBD, while rs962917 increased the risk of IBD, CD and UC in Caucasian populations. 27556856

2016

dbSNP: rs1545620
rs1545620
0.060 GeneticVariation BEFREE Although no association was found with ulcerative colitis in the comparison between the subgroups, the frequencies of rs962917 and rs1545620 were different in the Crohn's disease (CD) subgroup with ileocolitis (CC vs CT and TT, P = 0.014; and AA vs AC and CC, P = 0.022, respectively). rs1545620 variants appear to be the genetic susceptibility factor for perianal disease in CD patients (AA vs AC CC, P = 0.029). 24966617

2014

dbSNP: rs1545620
rs1545620
0.060 GeneticVariation BEFREE SNP rs1545620 is a non-synonymous SNP previously suspected to impact on ulcerative colitis. 24386489

2013

dbSNP: rs1545620
rs1545620
0.060 GeneticVariation BEFREE In addition to the IL2/IL21 locus, we observed association of the TT genotype of SNP rs1545620 in MYO9B with UC (P = 0.0169; OR = 0.29, 95% CI 0.11-0.78) and association of rs17375018 in IL23R with pancolitis in Chinese UC patients (P = 0.002; OR = 2.38, 95% CI 1.41-4.02). 21648020

2011

dbSNP: rs1545620
rs1545620
0.060 GeneticVariation BEFREE A nonsynonymous single nucleotide polymorphism (SNP) rs1545620 at the 3' end of the gene was found to be significantly associated with UC and weakly associated with Crohn's disease (CD). 19235913

2009