{{Rsnum
|rsid=3815087
|Gene=PSORS1C1
|Chromosome=6
|position=31125810
|Orientation=minus
|GMAF=0.2769
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=PSORS1C1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 68.1 | 29.2 | 2.7
| HCB | 42.3 | 44.5 | 13.1
| JPT | 59.3 | 37.2 | 3.5
| YRI | 49.0 | 44.2 | 6.8
| ASW | 52.6 | 31.6 | 15.8
| CHB | 42.3 | 44.5 | 13.1
| CHD | 46.3 | 45.4 | 8.3
| GIH | 26.7 | 50.5 | 22.8
| LWK | 29.1 | 52.7 | 18.2
| MEX | 62.1 | 36.2 | 1.7
| MKK | 19.2 | 49.4 | 31.4
| TSI | 44.6 | 44.6 | 10.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20041166
|Trait=HIV-1 control
|Title=Common Genetic Variation and the Control of HIV-1 in Human
|RiskAllele=
|Pval=8E-8
|OR=NR
|ORtxt=NR
|OA=1
}}

{{PMID Auto GWAS
|PMID=21801394
|Trait=None
|Title=Genome-Wide Association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe.
|RiskAllele=A
|Pval=3E-7
|OR=1.5300
|ORtxt=[1.29-1.80]
|OA=1
}}

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