{{Rsnum
|rsid=8057394
|Gene=GRIN2A
|Chromosome=16
|position=10021631
|Orientation=plus
|GMAF=0.41
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene_s=GRIN2A
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 7.7 | 43.1 | 49.2
| HCB | 24.4 | 62.2 | 13.3
| JPT | 31.1 | 42.2 | 26.7
| YRI | 38.1 | 46.0 | 15.9
| ASW | 0.0 | 0.0 | 0.0
| CHB | 24.4 | 62.2 | 13.3
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{omim
|desc=HUNTINGTON DISEASE; HD
|id=143100
|rsnum=8057394
}}

{{PMID Auto
|PMID=17569088
|Title=NR2A and NR2B receptor gene variations modify age at onset in Huntington disease in a sex-specific manner.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}