{{Rsnum
|rsid=7616215
|Chromosome=3
|position=46164194
|Orientation=plus
|GMAF=0.3242
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 15.9 | 41.6 | 42.5
| HCB | 0.7 | 30.7 | 68.6
| JPT | 6.2 | 25.7 | 68.1
| YRI | 20.4 | 43.5 | 36.1
| ASW | 22.8 | 47.4 | 29.8
| CHB | 0.7 | 30.7 | 68.6
| CHD | 0.0 | 22.0 | 78.0
| GIH | 21.8 | 52.5 | 25.7
| LWK | 37.3 | 48.2 | 14.5
| MEX | 1.7 | 36.2 | 62.1
| MKK | 53.2 | 42.3 | 4.5
| TSI | 9.8 | 41.2 | 49.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23291587
  |Trait=Behcet's disease
  |Title=Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1.
  |RiskAllele=C
  |Pval=4E-13
  |OR=1.39
  |ORtxt=[1.27-1.52]
  |OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}