{{Rsnum
|rsid=1585471
|Chromosome=4
|position=111781479
|Orientation=plus
|GMAF=0.3503
|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 | 39.8 | 48.7 | 11.5
| HCB | 29.4 | 50.7 | 19.9
| JPT | 21.4 | 56.2 | 22.3
| YRI | 50.7 | 41.1 | 8.2
| ASW | 43.9 | 47.4 | 8.8
| CHB | 29.4 | 50.7 | 19.9
| CHD | 25.7 | 52.3 | 22.0
| GIH | 28.7 | 50.5 | 20.8
| LWK | 51.8 | 42.7 | 5.5
| MEX | 46.6 | 43.1 | 10.3
| MKK | 47.4 | 39.1 | 13.5
| TSI | 37.3 | 51.0 | 11.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21505071
|Trait=None
|Title=A genome-wide association study reveals association between common variants in an intergenic region of 4q25 and high-grade myopia in the Chinese Han population.
|RiskAllele=
|Pval=0.000002
|OR=1.1500
|ORtxt=[1.09-1.22]
}}

{{PMID Auto
|PMID=22150588
|Title=Common variants in chromosome 4q25 are associated with myopia in Chinese adults.
}}

{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}