{{Rsnum
|rsid=3771863
|Gene=TACR1
|Chromosome=2
|position=75192588
|Orientation=plus
|GMAF=0.3173
|Gene_s=TACR1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 66.4 | 31.9 | 1.8
| HCB | 47.8 | 40.3 | 11.9
| JPT | 41.6 | 46.0 | 12.4
| YRI | 7.5 | 39.0 | 53.4
| ASW | 8.8 | 56.1 | 35.1
| CHB | 47.8 | 40.3 | 11.9
| CHD | 44.9 | 47.7 | 7.5
| GIH | 45.5 | 44.6 | 9.9
| LWK | 15.6 | 45.0 | 39.4
| MEX | 73.7 | 24.6 | 1.8
| MKK | 15.6 | 55.2 | 29.2
| TSI | 66.7 | 32.4 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23471985
  |Trait=Brain connectivity
  |Title=Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity.
  |RiskAllele=
  |Pval=3E-9
  |OR=NR
  |ORtxt=NR
  |OA=1
}}

{{PMID Auto
|PMID=17448763
|Title=Application of HapMap data to the evaluation of 8 candidate genes for pediatric slow transit constipation.
}}

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