Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs924080
rs924080
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.840 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
dbSNP: rs1518111
rs1518111
IL10 ; IL19
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.830 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
dbSNP: rs1800871
rs1800871
IL10 ; IL19
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.830 GeneticVariation GWASDB Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. 23291587

2013
dbSNP: rs1800871
rs1800871
IL10 ; IL19
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		T 0.830 GeneticVariation GWASDB Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behçet's disease susceptibility loci. 20622879

2010
dbSNP: rs1495965
rs1495965
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		G 0.820 GeneticVariation GWASDB Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behçet's disease susceptibility loci. 20622879

2010
dbSNP: rs17482078
rs17482078
ERAP1 ; LOC102724748
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		T 0.820 GeneticVariation GWASDB Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. 23291587

2013
dbSNP: rs2617170
rs2617170
KLRC4 ; KLRC4-KLRK1
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		T 0.820 GeneticVariation GWASDB Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. 23291587

2013
dbSNP: rs17810546
rs17810546
IL12A-AS1
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		A 0.810 GeneticVariation GWASDB Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. 23291587

2013
dbSNP: rs7574070
rs7574070
STAT4
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		A 0.810 GeneticVariation GWASDB Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. 23291587

2013
dbSNP: rs7574070
rs7574070
STAT4
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.810 GeneticVariation GWASDB Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997

2012
dbSNP: rs7616215
rs7616215
CCR3 ; LOC105377067
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		C 0.810 GeneticVariation GWASDB Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. 23291587

2013
dbSNP: rs17006292
rs17006292
TFCP2L1
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.800 GeneticVariation GWASDB Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997

2012
dbSNP: rs4947296
rs4947296
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.800 GeneticVariation GWASDB Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behcet's disease. 23041938

2013
dbSNP: rs4947296
rs4947296
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.800 GeneticVariation GWASDB Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997

2012
dbSNP: rs4959053
rs4959053
PSORS1C1
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.800 GeneticVariation GWASDB Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behcet's disease. 23041938

2013
dbSNP: rs4959053
rs4959053
PSORS1C1
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.800 GeneticVariation GWASDB Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997

2012
dbSNP: rs7572482
rs7572482
STAT4
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.800 GeneticVariation GWASDB Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997

2012
dbSNP: rs897200
rs897200
STAT4
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.800 GeneticVariation GWASDB Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997

2012
dbSNP: rs9266406
rs9266406
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.800 GeneticVariation GWASDB Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behcet's disease. 23041938

2013
dbSNP: rs9266406
rs9266406
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.800 GeneticVariation GWASDB Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997

2012
dbSNP: rs1608157
rs1608157
LOC107986860
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.710 GeneticVariation GWASDB Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behcet's disease. 23041938

2013
dbSNP: rs3024490
rs3024490
IL10 ; IL19
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.710 GeneticVariation GWASDB Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. 23291587

2013
dbSNP: rs10236188
rs10236188
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
dbSNP: rs10256482
rs10256482
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
dbSNP: rs10277380
rs10277380
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