{{Rsnum
|rsid=2836061
|Chromosome=21
|position=37952931
|Orientation=plus
|GMAF=0.2677
|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 | 69.0 | 27.4 | 3.5
| HCB | 64.2 | 33.6 | 2.2
| JPT | 75.2 | 23.0 | 1.8
| YRI | 10.9 | 49.0 | 40.1
| ASW | 29.8 | 54.4 | 15.8
| CHB | 64.2 | 33.6 | 2.2
| CHD | 66.1 | 31.2 | 2.8
| GIH | 71.3 | 27.7 | 1.0
| LWK | 17.8 | 50.5 | 31.8
| MEX | 58.6 | 37.9 | 3.4
| MKK | 12.2 | 49.4 | 38.5
| TSI | 72.5 | 25.5 | 2.0
| HapMapRevision=28
}}This SNP was associated with amyotrophic lateral sclerosis ([[ALS]]) based on a study of 1,152 patients.{{PMID|17671248}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}