Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs962917
rs962917
0.020 GeneticVariation BEFREE The rs962917 single nucleotide polymorphism (SNP) increased the risk of IBD, CD and UC. 27556856

2016

dbSNP: rs962917
rs962917
0.020 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