{{Rsnum
|rsid=7580332
|Chromosome=2
|position=18359378
|Orientation=plus
|GMAF=0.3512
|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 | 30.1 | 50.4 | 19.5
| HCB | 41.2 | 47.8 | 11.0
| JPT | 50.4 | 43.4 | 6.2
| YRI | 58.2 | 34.2 | 7.5
| ASW | 70.2 | 28.1 | 1.8
| CHB | 41.2 | 47.8 | 11.0
| CHD | 42.6 | 38.9 | 18.5
| GIH | 42.6 | 50.5 | 6.9
| LWK | 64.5 | 30.9 | 4.5
| MEX | 32.8 | 48.3 | 19.0
| MKK | 46.1 | 44.8 | 9.1
| TSI | 42.2 | 44.1 | 13.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=18084291
|Trait=Amyotrophic lateral sclerosis
|Title=Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis
|RiskAllele=
|Pval=0.0000090000000000000002
|OR=1.22
|ORtxt=[1.09-1.35]
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs7580332
|overall_frequency_n=34
|overall_frequency_d=128
|overall_frequency=0.265625
|n_genomes=26
|n_genomes_annotated=0
|n_haplomes=33
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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