{{Rsnum
|rsid=12541
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ESAM
|position=124753596
|Gene_s=ESAM,VSIG2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 60.2 | 35.4 | 4.4
| HCB | 54.4 | 40.4 | 5.1
| JPT | 46.9 | 41.6 | 11.5
| YRI | 2.0 | 25.9 | 72.1
| ASW | 8.8 | 49.1 | 42.1
| CHB | 54.4 | 40.4 | 5.1
| CHD | 54.1 | 43.1 | 2.8
| GIH | 64.0 | 31.0 | 5.0
| LWK | 3.7 | 36.1 | 60.2
| MEX | 66.7 | 31.6 | 1.8
| MKK | 5.2 | 49.7 | 45.1
| TSI | 61.8 | 33.3 | 4.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=24098564
|Title=The impact of genome-wide supported schizophrenia risk variants in the neurogranin gene on brain structure and function
}}

{{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}}