{{Rsnum
|rsid=4799088
|Chromosome=18
|position=79813548
|Orientation=plus
|GMAF=0.376
|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 | 55.8 | 38.1 | 6.2
| HCB | 34.3 | 46.0 | 19.7
| JPT | 28.3 | 52.2 | 19.5
| YRI | 29.9 | 47.6 | 22.4
| ASW | 42.1 | 40.4 | 17.5
| CHB | 34.3 | 46.0 | 19.7
| CHD | 38.5 | 47.7 | 13.8
| GIH | 31.7 | 50.5 | 17.8
| LWK | 27.3 | 47.3 | 25.5
| MEX | 34.5 | 41.4 | 24.1
| MKK | 21.8 | 51.3 | 26.9
| TSI | 67.6 | 28.4 | 3.9
| 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=
|Pval=0.000009
|OR=1.1500
|ORtxt=[NR]
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}