CCR3, C-C motif chemokine receptor 3, 1232

N. diseases: 8; N. variants: 6
Disease: Behcet Syndrome ×
Source: GWASDB ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.120 GeneticVariation disease GWASDB Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. 23291587 2013