{{Rsnum
|rsid=2285803
|Gene=PSORS1C1
|Chromosome=6
|position=31139481
|Orientation=minus
|GMAF=0.2727
|Gene_s=PSORS1C1,PSORS1C2
|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 | 8.8 | 37.2 | 54.0
| HCB | 8.8 | 43.8 | 47.4
| JPT | 11.5 | 46.9 | 41.6
| YRI | 6.1 | 36.7 | 57.1
| ASW | 10.5 | 50.9 | 38.6
| CHB | 8.8 | 43.8 | 47.4
| CHD | 11.0 | 45.0 | 44.0
| GIH | 5.0 | 46.5 | 48.5
| LWK | 5.5 | 39.1 | 55.5
| MEX | 6.9 | 41.4 | 51.7
| MKK | 3.8 | 38.5 | 57.7
| TSI | 8.8 | 42.2 | 49.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=24449210
|Title=Inherited genetic susceptibility to monoclonal gammopathy of unknown significance
}}

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