Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs723080
rs723080
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		C 0.700 GeneticVariation GWASCAT LRRK2 but not ATG16L1 is associated with Paneth cell defect in Japanese Crohn's disease patients. 28352666

2017
dbSNP: rs147629807
rs147629807
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASCAT LRRK2 but not ATG16L1 is associated with Paneth cell defect in Japanese Crohn's disease patients. 28352666

2017
dbSNP: rs12481514
rs12481514
ADRA1D
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		A 0.700 GeneticVariation GWASCAT LRRK2 but not ATG16L1 is associated with Paneth cell defect in Japanese Crohn's disease patients. 28352666

2017
dbSNP: rs116855232
rs116855232
NUDT15
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		T 0.730 GeneticVariation GWASCAT A common missense variant in NUDT15 confers susceptibility to thiopurine-induced leukopenia. 25108385

2014
dbSNP: rs9267911
rs9267911
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		T 0.800 GeneticVariation GWASCAT A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population. 23266558

2013
dbSNP: rs7329174
rs7329174
ELF1
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		G 0.800 GeneticVariation GWASCAT A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population. 23266558

2013
dbSNP: rs72981516
rs72981516
FCHSD2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		T 0.800 GeneticVariation GWASCAT A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population. 23266558

2013
dbSNP: rs3094188
rs3094188
POU5F1 ; PSORS1C3
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		C 0.800 GeneticVariation GWASCAT A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population. 23266558

2013
dbSNP: rs1487630
rs1487630
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		T 0.800 GeneticVariation GWASCAT A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population. 23266558

2013
dbSNP: rs11894081
rs11894081
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		T 0.800 GeneticVariation GWASCAT A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population. 23266558

2013
dbSNP: rs76418789
rs76418789
IL23R ; C1orf141
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.850 GeneticVariation GWASCAT A Genome-wide Association Study Identifying RAP1A as a Novel Susceptibility Gene for Crohn's Disease in Japanese Individuals. 30500874

2019
dbSNP: rs224136
rs224136
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.810 GeneticVariation GWASCAT A Genome-wide Association Study Identifying RAP1A as a Novel Susceptibility Gene for Crohn's Disease in Japanese Individuals. 30500874

2019
dbSNP: rs78898421
rs78898421
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASCAT A Genome-wide Association Study Identifying RAP1A as a Novel Susceptibility Gene for Crohn's Disease in Japanese Individuals. 30500874

2019
dbSNP: rs73243351
rs73243351
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASCAT A Genome-wide Association Study Identifying RAP1A as a Novel Susceptibility Gene for Crohn's Disease in Japanese Individuals. 30500874

2019
dbSNP: rs56354901
rs56354901
IL27
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASCAT A Genome-wide Association Study Identifying RAP1A as a Novel Susceptibility Gene for Crohn's Disease in Japanese Individuals. 30500874

2019
dbSNP: rs56167332
rs56167332
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASCAT A Genome-wide Association Study Identifying RAP1A as a Novel Susceptibility Gene for Crohn's Disease in Japanese Individuals. 30500874

2019
dbSNP: rs488200
rs488200
INKA2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		T 0.700 GeneticVariation GWASCAT A Genome-wide Association Study Identifying RAP1A as a Novel Susceptibility Gene for Crohn's Disease in Japanese Individuals. 30500874

2019
dbSNP: rs184950714
rs184950714
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 GeneticVariation GWASCAT A Genome-wide Association Study Identifying RAP1A as a Novel Susceptibility Gene for Crohn's Disease in Japanese Individuals. 30500874

2019
dbSNP: rs11209026
rs11209026
IL23R
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		G 0.900 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: rs2076756
rs2076756
NOD2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		G 0.830 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: rs4820425
rs4820425
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		A 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: rs3792109
rs3792109
ATG16L1 ; SCARNA5
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		A 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
IFNGR2
CUI: C0010346
Disease: Crohn 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: rs11742570
rs11742570
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		C 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: rs2241880
rs2241880
ATG16L1 ; SCARNA5
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		G 0.900 GeneticVariation GWASCAT A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. 22412388

2012