Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17482078
rs17482078
ERAP1 ; LOC102724748
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.820 GeneticVariation BEFREE Although preliminary, our data show a stronger association of rs17482078 with BS compa</span>red to rs27044 by means of case-control genetic analysis and bioinformatics prediction of protein structure change. 30820838

2019
dbSNP: rs17482078
rs17482078
ERAP1 ; LOC102724748
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.820 GeneticVariation BEFREE Our aim was, the replication in the Spanish population of the association described in the Turkish population between ERAP1 (rs17482078) and BD. 25019531

2014
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: rs17482078
rs17482078
ERAP1 ; LOC102724748
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		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