{{Rsnum
|rsid=17027230
|Chromosome=2
|position=102462870
|Orientation=plus
|GMAF=0.2727
|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 | 52.3 | 36.9 | 10.8
| HCB | 43.2 | 43.2 | 13.6
| JPT | 18.2 | 63.6 | 18.2
| YRI | 61.9 | 34.9 | 3.2
| ASW | 0.0 | 0.0 | 0.0
| CHB | 43.2 | 43.2 | 13.6
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}

This SNP was associated with amyotrophic lateral sclerosis ([[ALS]]) based on a study of 1,152 patients.{{PMID|17671248}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}