{{Rsnum
|rsid=284489
|Chromosome=8
|position=104945792
|Orientation=plus
|GMAF=0.4435
|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 | 41.6 | 45.1 | 13.3
| HCB | 35.0 | 49.6 | 15.3
| JPT | 30.1 | 51.3 | 18.6
| YRI | 9.5 | 43.5 | 46.9
| ASW | 5.3 | 57.9 | 36.8
| CHB | 35.0 | 49.6 | 15.3
| CHD | 35.8 | 48.6 | 15.6
| GIH | 58.4 | 33.7 | 7.9
| LWK | 11.0 | 38.5 | 50.5
| MEX | 39.7 | 50.0 | 10.3
| MKK | 23.1 | 43.6 | 33.3
| TSI | 61.8 | 30.4 | 7.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22570617
|Trait=None
|Title=Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.
|RiskAllele=
|Pval=9E-10
|OR=1.6100
|ORtxt=None
|OA=1
}}

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