{{Rsnum
|rsid=16887244
|Gene=LSM1
|Chromosome=8
|position=38173827
|Orientation=plus
|GMAF=0.2466
|Gene_s=LSM1
|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 | 51.3 | 39.8 | 8.8
| HCB | 43.8 | 44.5 | 11.7
| JPT | 42.5 | 46.0 | 11.5
| YRI | 76.2 | 22.4 | 1.4
| ASW | 71.9 | 24.6 | 3.5
| CHB | 43.8 | 44.5 | 11.7
| CHD | 41.3 | 44.0 | 14.7
| GIH | 82.2 | 16.8 | 1.0
| LWK | 74.5 | 23.6 | 1.8
| MEX | 65.5 | 29.3 | 5.2
| MKK | 69.2 | 28.8 | 1.9
| TSI | 50.0 | 44.1 | 5.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22037555
|Trait=None
|Title=Common variants on 8p12 and 1q24.2 confer risk of schizophrenia.
|RiskAllele=
|Pval=1E-10
|OR=1.1900
|ORtxt=None
|OA=1
}}

{{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}}