{{Rsnum
|rsid=9390754
|Gene=GRIK2
|Chromosome=6
|position=101517038
|Orientation=plus
|GMAF=0.2663
|Gene_s=GRIK2
|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 | 77.0 | 23.0 | 0.0
| HCB | 40.9 | 45.3 | 13.9
| JPT | 40.7 | 46.9 | 12.4
| YRI | 21.1 | 55.1 | 23.8
| ASW | 42.1 | 45.6 | 12.3
| CHB | 40.9 | 45.3 | 13.9
| CHD | 39.4 | 46.8 | 13.8
| GIH | 44.6 | 43.6 | 11.9
| LWK | 32.7 | 54.5 | 12.7
| MEX | 57.9 | 38.6 | 3.5
| MKK | 57.1 | 37.2 | 5.8
| TSI | 79.4 | 19.6 | 1.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=22116939
|Title=Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese
}}

{{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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}