Source: ALL

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 BEFREE Interestingly, we have found, majority of the tribal populations have low frequency of VL ('A' of rs3024498); and high frequency of leprosy ('T' of rs1554286), and Behcet's ('A' of rs1518111) associated alleles, whereas these were vice versa in castes. 25941808

2015
dbSNP: rs1518111
rs1518111
IL10 ; IL19
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.830 GeneticVariation BEFREE Similarly, rs1518111, which showed strong linkage disequilibrium (r(2)=1) with allele rs1800871, was also associated with BD (pc=0.026). 24269690

2014
dbSNP: rs1518111
rs1518111
IL10 ; IL19
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.830 GeneticVariation BEFREE In IL10, rs1518111 was nominally associated with BD before and after adjustment for population stratification (odds ratio [OR] for T allele 1.20, 95% confidence interval [95% CI] 1.02-1.40, unadjusted P [P(unadj) ] = 2.53 × 10(-2) ; adjusted P [P(adj) ] = 1.43 × 10(-2) ), and rs1554286 demonstrated a trend toward association (P(unadj) = 6.14 × 10(-2) ; P(adj) = 3.21 × 10(-2) ). 22378604

2012
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: rs1518111
rs1518111
IL10 ; IL19
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.830 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