{{Rsnum
|rsid=10861032
|Chromosome=12
|position=103518728
|Orientation=plus
|GMAF=0.2847
|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 | 1.8 | 25.7 | 72.6
| HCB | 25.5 | 47.4 | 27.0
| JPT | 21.2 | 58.4 | 20.4
| YRI | 21.8 | 42.2 | 36.1
| ASW | 10.5 | 45.6 | 43.9
| CHB | 25.5 | 47.4 | 27.0
| CHD | 21.1 | 39.4 | 39.4
| GIH | 23.8 | 40.6 | 35.6
| LWK | 17.3 | 49.1 | 33.6
| MEX | 1.7 | 25.9 | 72.4
| MKK | 6.4 | 37.8 | 55.8
| TSI | 2.9 | 23.5 | 73.5
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21878436
|Trait=None
|Title=A genome-wide association study identifies a region at chromosome 12 as a potential susceptibility locus for restenosis after percutaneous coronary intervention.
|RiskAllele=C
|Pval=1E-7
|OR=None
|ORtxt=None
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}
{{on chip | NatGeo2}}