{{Rsnum
|rsid=3094188
|Gene=PSORS1C3
|Chromosome=6
|position=31174468
|Orientation=minus
|GMAF=0.281
|Gene_s=PSORS1C3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 12.4 | 44.2 | 43.4
| HCB | 5.1 | 38.7 | 56.2
| JPT | 8.8 | 34.5 | 56.6
| YRI | 6.8 | 34.2 | 58.9
| ASW | 7.0 | 31.6 | 61.4
| CHB | 5.1 | 38.7 | 56.2
| CHD | 4.6 | 42.6 | 52.8
| GIH | 10.9 | 48.5 | 40.6
| LWK | 6.4 | 29.1 | 64.5
| MEX | 8.8 | 47.4 | 43.9
| MKK | 7.1 | 43.6 | 49.4
| TSI | 10.8 | 42.2 | 47.1
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23266558
  |Trait=Crohn's disease
  |Title=A Genome-Wide Association Study Identifies 2 Susceptibility Loci for Crohn's Disease in a Japanese Population.
  |RiskAllele=C
  |Pval=7E-7
  |OR=1.61
  |ORtxt=[1.33-1.94]
  }}

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