{{Rsnum
|rsid=1470407
|Chromosome=1
|position=59249320
|Orientation=plus
|GMAF=0.2117
|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 | 79.7 | 18.8 | 1.6
| HCB | 70.5 | 27.3 | 2.3
| JPT | 72.1 | 27.9 | 0.0
| YRI | 29.0 | 43.5 | 27.4
| ASW | 0.0 | 0.0 | 0.0
| CHB | 70.5 | 27.3 | 2.3
| 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
}}[[rs1470407]] is one of 6 SNPs found upstream of an (uncharacterized) gene known as FLJ10986 that have been found to be overrepresented in 1,152 patients with sporadic amyotrophic lateral sclerosis ([[ALS]]).{{PMID|17671248}}

{{PMID|19177248}} A study involving a large case-control series from the Netherlands, Belgium, Sweden and Ireland (total: 1883 sporadic ALS patients and 2063 controls) found no significant association between sporadic ALS and the six previously reported associated SNPs, including this one.

{{PMID Auto
|PMID=19922138
|Title=Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosis
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}