{{Rsnum
|rsid=351240
|Gene=STRA6
|Chromosome=15
|position=74182504
|Orientation=plus
|GMAF=0.008724
|Gene_s=STRA6
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 99.1 | 0.9 | 0.0
| HCB | 99.3 | 0.7 | 0.0
| JPT | 99.1 | 0.9 | 0.0
| YRI | 92.4 | 7.6 | 0.0
| ASW | 98.2 | 1.8 | 0.0
| CHB | 99.3 | 0.7 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 89.9 | 10.1 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 88.1 | 11.9 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=24004541
|Title=Association study of TLR-9 polymorphisms and systemic lupus erythematosus in Northern Chinese Han population
}}

{{PMID Auto
|PMID=17503335
|Title=Matthew-Wood syndrome is caused by truncating mutations in the retinol-binding protein receptor gene STRA6.
|OA=1
}}

{{on chip | Illumina Human 1M}}