Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs924080
rs924080
0.840 GeneticVariation BEFREE Of these 5 loci, 2 were found to be significantly associated with BD susceptibility: rs17375018 (G vs. A, OR = 1.50, 95% CI: 1.34-1.68, <i>P</i> < .00001) and rs924080 (T vs. C, OR = 1.36, 95% CI: 1.29-1.43, <i>P</i> < .00001). 31814470

2019

dbSNP: rs924080
rs924080
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: rs924080
rs924080
0.840 GeneticVariation BEFREE SNPs (rs924080 and rs11209032) of the IL23R-IL12RB2 region were found to be associated with BD in a Northern Chinese Han population. 27660093

2016

dbSNP: rs924080
rs924080
0.840 GeneticVariation BEFREE Our findings not only confirmed the association of IL10/rs1800871 and IL23R-IL12RB2/rs924080 with BD but also identified 2 susceptibility single nucleotide polymorphisms in IL10 and IL23R-IL12RB2 (rs3024490 and rs12141431) with BD in Han Chinese. 27464962

2017

dbSNP: rs924080
rs924080
0.840 GeneticVariation BEFREE Six SNPs in IL23R-IL12RB2 were found to be associated with BD after Bonferroni correction for multiple testing, the most significant of which were rs17375018 (OR for G allele 1.51, 95% CI 1.27-1.78, P(unadj) = 1.93 × 10(-6) ), rs7517847 (OR for T allele 1.48, 95% CI 1.26-1.74, P(unadj) = 1.23 × 10(-6) ), and rs924080 (OR for T allele 1.29, 95% CI 1.20-1.39, P = 1.78 × 10(-5) ). 22378604

2012

dbSNP: rs924080
rs924080
0.840 GeneticVariation GWASCAT Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease. 20622878

2010

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
0.820 GeneticVariation BEFREE An IL23R-IL12RB2 intergenic SNP rs1495965 was significantly associated with BD risk (OR (95% CI) = 1.5 (1.3, 1.7), P = 2.5 × 10<sup>-7</sup>) in the pooled meta-analysis of the discovery (1.4 (1.2, 1.7), P = 4.9 × 10<sup>-7</sup>) and replication (1.9 (1.3, 2.6), P = 6.0 × 10<sup>-4</sup>) phases. 29017598

2017

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

2013

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

2013

dbSNP: rs10236188
rs10236188
0.700 GeneticVariation GWASDB Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behcet's disease. 23041938

2013

dbSNP: rs10256482
rs10256482
0.700 GeneticVariation GWASDB Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behcet's disease. 23041938

2013

dbSNP: rs10277380
rs10277380
0.700 GeneticVariation GWASDB Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behcet's disease. 23041938

2013

dbSNP: rs1522596
rs1522596
0.700 GeneticVariation GWASDB Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behcet's disease. 23041938

2013

dbSNP: rs1916012
rs1916012
0.700 GeneticVariation GWASDB Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behcet's disease. 23041938

2013

dbSNP: rs2253907
rs2253907
0.700 GeneticVariation GWASDB Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behcet's disease. 23041938

2013

dbSNP: rs2253907
rs2253907
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

dbSNP: rs2517411
rs2517411
0.700 GeneticVariation GWASDB Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behcet's disease. 23041938

2013

dbSNP: rs2848479
rs2848479
A 0.700 GeneticVariation GWASCAT Genetic Analysis with the Immunochip Platform in Behçet Disease. Identification of Residues Associated in the HLA Class I Region and New Susceptibility Loci. 27548383

2016