{{Rsnum
|rsid=1411478
|Gene=STX6
|Chromosome=1
|position=180993146
|Orientation=plus
|GMAF=0.4256
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=STX6
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 23.0 | 48.7 | 28.3
| HCB | 8.8 | 50.4 | 40.9
| JPT | 9.7 | 44.2 | 46.0
| YRI | 30.8 | 50.7 | 18.5
| ASW | 15.8 | 57.9 | 26.3
| CHB | 8.8 | 50.4 | 40.9
| CHD | 12.8 | 49.5 | 37.6
| GIH | 38.6 | 46.5 | 14.9
| LWK | 35.5 | 51.8 | 12.7
| MEX | 14.0 | 43.9 | 42.1
| MKK | 18.6 | 53.8 | 27.6
| TSI | 20.6 | 43.1 | 36.3
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21685912
|Trait=None
|Title=Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
|RiskAllele=
|Pval=4E-11
|OR=1.2700
|ORtxt=[1.19-1.37]
|OA=1
}}

{{PMID Auto
|PMID=23415606
|Title=STX6 rs1411478 is not associated with increased risk of Parkinson's disease
}}

{{PMID Auto
|PMID=23116876
|Title=An exploratory study on STX6, MOBP, MAPT, and EIF2AK3 and late-onset Alzheimer's disease.
}}

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