{{Rsnum
|rsid=28489906
|Gene=GRIN1
|Chromosome=9
|position=137143947
|Orientation=plus
|GMAF=0.3586
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=GRIN1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 23.9 | 52.2 | 23.9
| HCB | 59.1 | 36.5 | 4.4
| JPT | 59.3 | 38.9 | 1.8
| YRI | 63.9 | 33.3 | 2.7
| ASW | 56.1 | 35.1 | 8.8
| CHB | 59.1 | 36.5 | 4.4
| CHD | 65.1 | 30.3 | 4.6
| GIH | 35.6 | 37.6 | 26.7
| LWK | 76.1 | 21.1 | 2.8
| MEX | 31.0 | 51.7 | 17.2
| MKK | 71.8 | 25.6 | 2.6
| TSI | 20.6 | 53.9 | 25.5
| 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 | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}