Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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: 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: 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: 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: 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: 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: 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: rs936551
rs936551
CPLX1
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
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: 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: 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: 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: 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: rs9368678
rs9368678
HLA-B ; LOC112267902
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: rs9268861
rs9268861
HLA-DRB9
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: rs9266409
rs9266409
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: rs7775759
rs7775759
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: rs6933050
rs6933050
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: rs6910516
rs6910516
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: rs3094584
rs3094584
MICA
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: rs2517411
rs2517411
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: rs2253907
rs2253907
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: rs1965673
rs1965673
WWC1
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: rs1916012
rs1916012
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