Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11190140
rs11190140
NKX2-3 ; LINC01475
0.810 GeneticVariation BEFREE For rs11190140 polymorphism (C/T) and CD risk, the risk estimate for the allele contrast was OR = 1.201 (1.136-1.269). 24473197

2014
dbSNP: rs11190140
rs11190140
NKX2-3 ; LINC01475
T 0.810 GeneticVariation GWASCAT Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 18587394

2008
dbSNP: rs11190140
rs11190140
NKX2-3 ; LINC01475
T 0.810 GeneticVariation GWASDB Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 18587394

2008