{{Rsnum
|rsid=13036957
|Chromosome=20
|position=43193056
|Orientation=plus
|GMAF=0.1956
|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 | 8.8 | 31.0 | 60.2
| HCB | 3.7 | 17.6 | 78.7
| JPT | 2.7 | 26.5 | 70.8
| YRI | 2.1 | 34.9 | 63.0
| ASW | 7.0 | 22.8 | 70.2
| CHB | 3.7 | 17.6 | 78.7
| CHD | 3.7 | 22.0 | 74.3
| GIH | 5.0 | 31.7 | 63.4
| LWK | 0.9 | 28.2 | 70.9
| MEX | 0.0 | 19.0 | 81.0
| MKK | 6.4 | 31.4 | 62.2
| TSI | 2.0 | 37.3 | 60.8
| 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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}