Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7848647
rs7848647
0.840 GeneticVariation BEFREE For rs7848647 polymorphism, significantly protective association between this polymorphism and CD risk was also observed, but not in UC. 29873318

2018

dbSNP: rs7848647
rs7848647
0.840 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007

2016

dbSNP: rs7848647
rs7848647
0.840 GeneticVariation BEFREE The CC genotype of rs6478108, AA genotype of rs4263839, the AA genotype of rs6478109, the TT genotype of rs7848647 and the CC genotype of rs7869487 were all protectively associated with CD but not with UC. 25501099

2014

dbSNP: rs7848647
rs7848647
0.840 GeneticVariation BEFREE According to the subgroup analysis by ethnicity, except for rs4263839 in Caucasian and rs4979462 in Asian, all the rest investigated TNFSF15 polymorphisms were associated with CD risk and rs3810936 and rs7848647 polymorphism in Asian as well as rs6478108 polymorphism in Caucasian were associated with UC risk. 25028192

2014

dbSNP: rs7848647
rs7848647
0.840 GeneticVariation BEFREE Carriers of three polymorphisms, including rs3810936, rs6478108, and rs7848647, showed statistically significant association with CD (adjusted OR [aOR] 2.81, 95% confidence interval [CI] 1.94-4.07, P= 4.4 x 10(-8); aOR 3.49, 95% CI 2.42-5.04, P= 2.7 x 10(-11); and aOR 3.49, 95% CI 2.42-5.03, P= 2.2 x 10(-11), respectively). 18422820

2008

dbSNP: rs7848647
rs7848647
0.840 GeneticVariation GWASDB Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease. 16221758

2005