Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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: 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