{{Rsnum
|rsid=8636
|Gene=SNAP25
|Chromosome=20
|position=10307094
|Orientation=plus
|GMAF=0.2704
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=SNAP25
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 38.9 | 46.0 | 15.0
| HCB | 63.2 | 32.4 | 4.4
| JPT | 43.8 | 48.2 | 8.0
| YRI | 67.3 | 28.6 | 4.1
| ASW | 75.4 | 21.1 | 3.5
| CHB | 63.2 | 32.4 | 4.4
| CHD | 59.3 | 35.2 | 5.6
| GIH | 55.4 | 36.6 | 7.9
| LWK | 68.5 | 28.7 | 2.8
| MEX | 55.2 | 43.1 | 1.7
| MKK | 65.8 | 33.5 | 0.6
| TSI | 44.1 | 48.0 | 7.8
| HapMapRevision=28
}}{{PMID Auto
|PMID=19132710
|Title=Evidence that putative ADHD low risk alleles at SNAP25 may increase the risk of schizophrenia
}}

{{PMID|21996783}} Role of SNAP25 explored in eastern Indian attention deficit hyperactivity disorder probands.

{{PMID Auto
|PMID=23593184
|Title=DNA variation in the SNAP25 gene confers risk to ADHD and is associated with reduced expression in prefrontal cortex.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}