{{Rsnum
|rsid=10493256
|Chromosome=1
|position=59223276
|Orientation=minus
|GMAF=0.1708
|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 | 9.9 | 45.9 | 44.1
| HCB | 1.5 | 29.9 | 68.6
| JPT | 6.3 | 20.7 | 73.0
| YRI | 0.0 | 10.9 | 89.1
| ASW | 0.0 | 22.8 | 77.2
| CHB | 1.5 | 29.9 | 68.6
| CHD | 2.9 | 31.4 | 65.7
| GIH | 0.0 | 0.0 | 0.0
| LWK | 1.9 | 8.3 | 89.8
| MEX | 1.8 | 28.1 | 70.2
| MKK | 0.7 | 33.6 | 65.8
| TSI | 2.9 | 25.5 | 71.6
| HapMapRevision=28
}}[[rs10493256]] 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|19125359}} appears to increase the risk of developing sporadic ALS in our Chinese population

{{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=19922123
|Title=Clinical and genetic features of patients with sporadic amyotrophic lateral sclerosis in south-west China
}}

{{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 | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}