Gene: FUT2 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs516246
rs516246
FUT2 ; LOC105447645
0.800 GeneticVariation GWASCAT Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. 28067908

2017
dbSNP: rs516246
rs516246
FUT2 ; LOC105447645
A 0.800 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919

2015
dbSNP: rs516246
rs516246
FUT2 ; LOC105447645
T 0.800 GeneticVariation GWASCAT Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. 23128233

2012
dbSNP: rs516246
rs516246
FUT2 ; LOC105447645
T 0.800 GeneticVariation GWASDB Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. 23128233

2012
dbSNP: rs504963
rs504963
FUT2 ; LOC105447645
A 0.800 GeneticVariation GWASCAT Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. 20570966

2010
dbSNP: rs504963
rs504963
FUT2 ; LOC105447645
A 0.800 GeneticVariation GWASDB Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. 20570966

2010
dbSNP: rs602662
rs602662
FUT2 ; LOC105447645
G 0.710 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688

2015
dbSNP: rs602662
rs602662
FUT2 ; LOC105447645
0.710 GeneticVariation BEFREE Further evidence of the relevance of this locus to CD pathogenesis was demonstrated by the association of the original four SNPs and CD in the recently published CD GWAS meta-analysis (rs602662, P=0.001). 20570966

2010
dbSNP: rs679574
rs679574
FUT2 ; LOC105447645
0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007

2016
dbSNP: rs1047781
rs1047781
FUT2 ; LOC105447645
0.020 GeneticVariation BEFREE The FUT2 non-secretor allele showed genome-wide significant association with CD in Koreans (rs1047781, odds ratio [OR] = 1.30, P<sub>combined</sub>  = 3.52 × 10<sup>-12</sup> ). 31260595

2020
dbSNP: rs601338
rs601338
FUT2 ; LOC105447645
0.020 GeneticVariation BEFREE Stratified by disease type, we found a significant association between rs601338 polymorphism with CD and UC in the Chinese population, but not in the white population. 30615603

2019
dbSNP: rs1047781
rs1047781
FUT2 ; LOC105447645
0.020 GeneticVariation BEFREE Our study strongly implicates the polymorphic locus of FUT2 (rs1047781) in CD susceptibility in Chinese population. 24720527

2014
dbSNP: rs601338
rs601338
FUT2 ; LOC105447645
0.020 GeneticVariation BEFREE The A allele of rs601338 showed nominal association with dominant protection from UC (P = 0.044, OR: 0.82) and UC+CD (P = 0.035, OR: 0.84). 23075394

2012