Source: GWASDB

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3586
Gene Symbol: IL10
IL10
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.700 GeneticVariation GWASDB Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. 23291587

2013
Entrez Id: 3106
Gene Symbol: HLA-B
HLA-B
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.700 GeneticVariation GWASDB Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behcet's disease. 23041938

2013
Entrez Id: 51752
Gene Symbol: ERAP1
ERAP1
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.700 GeneticVariation GWASDB Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. 23291587

2013
Entrez Id: 3106
Gene Symbol: HLA-B
HLA-B
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.700 GeneticVariation GWASDB Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997

2012
Entrez Id: 3586
Gene Symbol: IL10
IL10
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.700 GeneticVariation GWASDB Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease. 20622878

2010
Entrez Id: 3586
Gene Symbol: IL10
IL10
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.700 GeneticVariation GWASDB Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behçet's disease susceptibility loci. 20622879

2010
Entrez Id: 6775
Gene Symbol: STAT4
STAT4
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.670 GeneticVariation GWASDB Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. 23291587

2013
Entrez Id: 6775
Gene Symbol: STAT4
STAT4
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.670 GeneticVariation GWASDB Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997

2012
Entrez Id: 8302
Gene Symbol: KLRC4
KLRC4
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.630 GeneticVariation GWASDB Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. 23291587

2013
Entrez Id: 101928376
Gene Symbol: IL12A-AS1
IL12A-AS1
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.410 GeneticVariation GWASDB Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. 23291587

2013
Entrez Id: 170679
Gene Symbol: PSORS1C1
PSORS1C1
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.400 GeneticVariation GWASDB Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behcet's disease. 23041938

2013
Entrez Id: 170679
Gene Symbol: PSORS1C1
PSORS1C1
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.400 GeneticVariation GWASDB Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997

2012
Entrez Id: 100507436
Gene Symbol: MICA
MICA
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.200 GeneticVariation GWASDB Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behcet's disease. 23041938

2013
Entrez Id: 100528032
Gene Symbol: KLRC4-KLRK1
KLRC4-KLRK1
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.120 GeneticVariation GWASDB Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. 23291587

2013
Entrez Id: 1232
Gene Symbol: CCR3
CCR3
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.120 GeneticVariation GWASDB Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. 23291587

2013
Entrez Id: 4277
Gene Symbol: MICB
MICB
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.120 GeneticVariation GWASDB Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997

2012
Entrez Id: 29949
Gene Symbol: IL19
IL19
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.100 GeneticVariation GWASDB Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. 23291587

2013
Entrez Id: 23286
Gene Symbol: WWC1
WWC1
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.100 GeneticVariation GWASDB Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behcet's disease. 23041938

2013
Entrez Id: 3132
Gene Symbol: HLA-DRB9
HLA-DRB9
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.100 GeneticVariation GWASDB Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behcet's disease. 23041938

2013
Entrez Id: 1041
Gene Symbol: CDSN
CDSN
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.100 GeneticVariation GWASDB Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997

2012
Entrez Id: 54535
Gene Symbol: CCHCR1
CCHCR1
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.100 GeneticVariation GWASDB Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997

2012
Entrez Id: 29842
Gene Symbol: TFCP2L1
TFCP2L1
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.100 GeneticVariation GWASDB Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997

2012
Entrez Id: 29949
Gene Symbol: IL19
IL19
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.100 GeneticVariation GWASDB Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behçet's disease susceptibility loci. 20622879

2010
Entrez Id: 29949
Gene Symbol: IL19
IL19
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.100 GeneticVariation GWASDB Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease. 20622878

2010