{{Rsnum
|rsid=11601239
|Gene=GRIA4
|Chromosome=11
|position=105685872
|Orientation=plus
|GMAF=0.449
|Gene_s=GRIA4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 16.7 | 63.0 | 20.4
| HCB | 42.1 | 55.3 | 2.6
| JPT | 31.7 | 53.7 | 14.6
| YRI | 0.0 | 0.0 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 42.1 | 55.3 | 2.6
| 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
}}{{PMID Auto GWAS
  |PMID=23396134
  |Trait=Refractive error
  |Title=Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.
  |RiskAllele=C
  |Pval=6E-9
  |OR=.10
  |ORtxt=[0.064-0.126] unit decrease
  |OA=1
}}