Disease: Behcet Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17482078
rs17482078
Entrez Id: 51752;102724748
Gene Symbol: ERAP1;LOC102724748
ERAP1;LOC102724748
CUI: C0004943
Disease:
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
Entrez Id: 51752;102724748
Gene Symbol: ERAP1;LOC102724748
ERAP1;LOC102724748
CUI: C0004943
Disease:
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
Entrez Id: 51752;102724748
Gene Symbol: ERAP1;LOC102724748
ERAP1;LOC102724748
CUI: C0004943
Disease:
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
Entrez Id: 51752;102724748
Gene Symbol: ERAP1;LOC102724748
ERAP1;LOC102724748
CUI: C0004943
Disease:
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