{{Rsnum
|rsid=9390459
|Gene=STXBP5
|Chromosome=6
|position=147359223
|Orientation=plus
|GMAF=0.4835
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=STXBP5
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 16.8 | 54.9 | 28.3
| HCB | 54.7 | 40.1 | 5.1
| JPT | 49.6 | 39.8 | 10.6
| YRI | 15.6 | 47.6 | 36.7
| ASW | 17.5 | 56.1 | 26.3
| CHB | 54.7 | 40.1 | 5.1
| CHD | 50.5 | 42.2 | 7.3
| GIH | 19.8 | 40.6 | 39.6
| LWK | 24.5 | 44.5 | 30.9
| MEX | 25.9 | 48.3 | 25.9
| MKK | 21.8 | 49.4 | 28.8
| TSI | 19.6 | 48.0 | 32.4
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20231535
|Trait=Plasma coagulation factors
|Title=Novel Associations of Multiple Genetic Loci With Plasma Levels of Factor VII, Factor VIII, and von Willebrand Factor. The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium
|RiskAllele=A
|Pval=1E-22
|OR=4.80
|ORtxt=[2.1-7.5] % decrease
|OA=1
}}

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