{{Rsnum
|rsid=1488902
|Chromosome=11
|position=89611857
|Orientation=plus
|GMAF=0.3999
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 14.2 | 54.9 | 31.0
| HCB | 18.4 | 52.2 | 29.4
| JPT | 32.1 | 42.9 | 25.0
| YRI | 20.5 | 54.1 | 25.3
| ASW | 24.6 | 52.6 | 22.8
| CHB | 18.4 | 52.2 | 29.4
| CHD | 24.8 | 46.8 | 28.4
| GIH | 6.9 | 54.5 | 38.6
| LWK | 20.0 | 46.4 | 33.6
| MEX | 8.6 | 48.3 | 43.1
| MKK | 17.9 | 46.2 | 35.9
| TSI | 14.7 | 45.1 | 40.2
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20801717
|Trait=None
|Title=Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study
|RiskAllele=C
|Pval=0.000003
|OR=1.1450
|ORtxt=[NR]
|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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}