Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2617170
rs2617170
KLRC4 ; KLRC4-KLRK1
T 0.820 GeneticVariation GWASCAT Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. 23291587

2013
dbSNP: rs1495965
rs1495965 		0.820 GeneticVariation BEFREE SNPs rs10489629, rs1343151, and rs1495965 were also significantly associated with BD in all tests performed. 22378604

2012
dbSNP: rs1495965
rs1495965 		G 0.820 GeneticVariation GWASCAT Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behçet's disease susceptibility loci. 20622879

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

2010
dbSNP: rs17810546
rs17810546
IL12A-AS1
G 0.810 GeneticVariation GWASCAT Genome-wide association study in an admixed case series reveals IL12A as a new candidate in Behçet disease. 25799145

2015
dbSNP: rs17810546
rs17810546
IL12A-AS1
0.810 GeneticVariation BEFREE For all 6 SNPs tested by meta-analysis (Pmeta ), the association with BD was strengthened, because the direction and magnitude of association were similar across populations (e.g., for rs7574070, odds ratio [OR] for A allele 1.29 [95% confidence interval (95% CI) 1.21-1.37], Pmeta  = 2.34 × 10(-16) ; for rs7616215, OR for C allele 0.70 [95% CI 0.65-0.76], Pmeta  = 1.54 × 10(-19) ; for rs17810546, OR for A allele 0.60 [95% CI 0.52-0.70], Pmeta  = 6.34 × 10(-11) ; for rs2617170, OR for T allele 0.76 [95% CI 0.70-0.81], Pmeta  = 2.75 × 10(-14) ; for rs13154629, OR for TT genotype 2.76 [95% CI 2.01-3.80], Pmeta  = 3.57 × 10(-10) ). 26097239

2015
dbSNP: rs7574070
rs7574070
STAT4
0.810 GeneticVariation BEFREE For all 6 SNPs tested by meta-analysis (Pmeta ), the association with BD was strengthened, because the direction and magnitude of association were similar across populations (e.g., for rs7574070, odds ratio [OR] for A allele 1.29 [95% confidence interval (95% CI) 1.21-1.37], Pmeta  = 2.34 × 10(-16) ; for rs7616215, OR for C allele 0.70 [95% CI 0.65-0.76], Pmeta  = 1.54 × 10(-19) ; for rs17810546, OR for A allele 0.60 [95% CI 0.52-0.70], Pmeta  = 6.34 × 10(-11) ; for rs2617170, OR for T allele 0.76 [95% CI 0.70-0.81], Pmeta  = 2.75 × 10(-14) ; for rs13154629, OR for TT genotype 2.76 [95% CI 2.01-3.80], Pmeta  = 3.57 × 10(-10) ). 26097239

2015
dbSNP: rs7616215
rs7616215
CCR3 ; LOC105377067
0.810 GeneticVariation BEFREE Six SNPs (in decreasing order of significance, rs7616215 located 38 kb downstream of CCR1, rs2617170 [p.Asn104Ser] in KLRC4, rs17810546 in IL12A-AS1, rs7574070 in STAT4, and rs10050860 [p.Asp575Asn] and rs13154629 in ERAP1) were nominally associated with BD in both allelic association tests (5.05 × 10(-9) ≤ Pallele ≤ 7.55 × 10(-3) ) and sex-adjusted genotypic association tests (6.01 × 10(-9) ≤ adjusted P value ≤ 1.30 × 10(-2) ). 26097239

2015
dbSNP: rs17810546
rs17810546
IL12A-AS1
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
A 0.810 GeneticVariation GWASCAT 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
A 0.810 GeneticVariation GWASCAT 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
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: rs7616215
rs7616215
CCR3 ; LOC105377067
C 0.810 GeneticVariation GWASCAT 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
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
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: rs7574070
rs7574070
STAT4
T 0.810 GeneticVariation GWASCAT 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 		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
0.800 GeneticVariation GWASDB Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behcet's disease. 23041938

2013
dbSNP: rs9266406
rs9266406 		0.800 GeneticVariation GWASDB Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behcet's disease. 23041938

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

2012
dbSNP: rs17006292
rs17006292
TFCP2L1
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 		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 		0.800 GeneticVariation GWASCAT 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
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
0.800 GeneticVariation GWASCAT Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997

2012