Variant: rs7616215 

    present in Gene: CCR3;LOC105377067
    present in Chromosome: 3
    Position on Chromosome: 46164194
    Alleles of this Variant: C/T

rs7616215 in CCR3;LOC105377067 gene and Behcet Syndrome PMID 23291587 2013 Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1.

rs7616215 in CCR3;LOC105377067 gene and Celiac Disease PMID 22057235 2011 Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.