{{Rsnum
|rsid=2301364
|Gene=GRIN1
|Chromosome=9
|position=137140083
|Orientation=plus
|GMAF=0.1703
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=GRIN1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 1.8 | 16.8 | 81.4
| HCB | 3.6 | 37.2 | 59.1
| JPT | 6.2 | 36.3 | 57.5
| YRI | 3.4 | 24.1 | 72.4
| ASW | 1.8 | 19.3 | 78.9
| CHB | 3.6 | 37.2 | 59.1
| CHD | 5.5 | 33.9 | 60.6
| GIH | 8.9 | 46.5 | 44.6
| LWK | 5.5 | 31.2 | 63.3
| MEX | 1.7 | 37.9 | 60.3
| MKK | 3.2 | 16.0 | 80.8
| TSI | 1.0 | 24.5 | 74.5
| HapMapRevision=28
}}{{PMID Auto
|PMID=20438806
|Title=Association analysis of GRIN1 and GRIN2B polymorphisms and Parkinson's disease in a hospital-based case-control study
}}

{{on chip | Illumina Human 1M}}