NKX2-3, NK2 homeobox 3, 159296

N. diseases: 22; N. variants: 4
Disease: Crohn Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11190140
rs11190140
Entrez Id: 159296;101927324
Gene Symbol: NKX2-3;LINC01475
NKX2-3;LINC01475
CUI: C0010346
Disease:
Crohn Disease 		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
Entrez Id: 159296;101927324
Gene Symbol: NKX2-3;LINC01475
NKX2-3;LINC01475
CUI: C0010346
Disease:
Crohn Disease 		T 0.810 GeneticVariation GWASCAT Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 18587394 2008
dbSNP: rs11190140
rs11190140
Entrez Id: 159296;101927324
Gene Symbol: NKX2-3;LINC01475
NKX2-3;LINC01475
CUI: C0010346
Disease:
Crohn Disease 		T 0.810 GeneticVariation GWASDB Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 18587394 2008