{{Rsnum
|rsid=9369640
|Chromosome=6
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=PHACTR1
|position=12901209
|Gene_s=PHACTR1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 38.9 | 45.1 | 15.9
| HCB | 97.1 | 2.9 | 0.0
| JPT | 87.6 | 11.5 | 0.9
| YRI | 7.5 | 43.5 | 49.0
| ASW | 26.3 | 36.8 | 36.8
| CHB | 97.1 | 2.9 | 0.0
| CHD | 95.4 | 4.6 | 0.0
| GIH | 74.3 | 23.8 | 2.0
| LWK | 3.6 | 41.8 | 54.5
| MEX | 39.7 | 41.4 | 19.0
| MKK | 10.9 | 44.2 | 44.9
| TSI | 36.6 | 43.6 | 19.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=24262325
  |Trait=Coronary artery disease
  |Title=Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
  |RiskAllele=C
  |Pval=3E-11
  |OR=1.10
  |ORtxt=[1.08-1.14]
  }}

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