{{Rsnum
|rsid=10239794
|Gene=DPP6
|Chromosome=7
|position=154508809
|Orientation=plus
|GMAF=0.4642
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=DPP6
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 40.7 | 42.5 | 16.8
| HCB | 7.3 | 52.6 | 40.1
| JPT | 3.6 | 36.6 | 59.8
| YRI | 19.7 | 55.1 | 25.2
| ASW | 12.3 | 52.6 | 35.1
| CHB | 7.3 | 52.6 | 40.1
| CHD | 11.9 | 42.2 | 45.9
| GIH | 26.7 | 54.5 | 18.8
| LWK | 18.2 | 61.8 | 20.0
| MEX | 25.9 | 56.9 | 17.2
| MKK | 12.8 | 55.1 | 32.1
| TSI | 31.4 | 53.9 | 14.7
| HapMapRevision=28
}}[[rs10239794]], a SNP in the region of the [[DPP6]] gene on chromosome 7, has been associated with the sporadic form of [[ALS]] (Lou Gehrig's disease) in a study of 1000+ European patients. The odds ratio for the risk allele [[rs10239794(C)]] is 1.30 (CI: 1.18 - 1.43). {{PMID|18084291}}

A "CC" haplotype for this SNP and that of it's neighbor [[rs10260404]] is also highly (statistically; p=10e-9) associated with [[ALS]]. {{PMID|18084291}}

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