IFNGR2, interferon gamma receptor 2, 3460

N. diseases: 71; N. variants: 13
Disease: Crohn Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2834215
rs2834215
Entrez Id: 3460
Gene Symbol: IFNGR2
IFNGR2
CUI: C0010346
Disease:
Crohn Disease 		0.800 GeneticVariation GWASCAT A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300. 22936669 2013
dbSNP: rs2834215
rs2834215
Entrez Id: 3460
Gene Symbol: IFNGR2
IFNGR2
CUI: C0010346
Disease:
Crohn Disease 		0.800 GeneticVariation GWASDB A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300. 22936669 2013