{{Rsnum
|rsid=4959053
|Gene=PSORS1C1
|Chromosome=6
|position=31131800
|Orientation=plus
|GMAF=0.0652
|Gene_s=PSORS1C1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.9 | 15.9 | 83.2
| HCB | 0.7 | 16.8 | 82.5
| JPT | 1.8 | 15.9 | 82.3
| YRI | 0.0 | 1.4 | 98.6
| ASW | 0.0 | 3.5 | 96.5
| CHB | 0.7 | 16.8 | 82.5
| CHD | 2.8 | 22.9 | 74.3
| GIH | 0.0 | 32.7 | 67.3
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 12.1 | 87.9
| MKK | 0.0 | 1.3 | 98.7
| TSI | 1.0 | 15.7 | 83.3
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23001997
  |Trait=Behcet's disease
  |Title=Identification of a susceptibility locus in STAT4 for Beh&#x000e7;et's disease in Han Chinese in a genome-wide association study.
  |RiskAllele=
  |Pval=2E-20
  |OR=   4.38
  |ORtxt=[3.20-5.99] 
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}