{{Rsnum
|rsid=12347433
|Gene=TNC
|Chromosome=9
|position=115035318
|Orientation=plus
|GMAF=0.1754
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=TNC
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 6.2 | 38.1 | 55.8
| HCB | 7.3 | 28.5 | 64.2
| JPT | 0.0 | 23.9 | 76.1
| YRI | 0.0 | 8.2 | 91.8
| ASW | 1.8 | 29.8 | 68.4
| CHB | 7.3 | 28.5 | 64.2
| CHD | 0.9 | 22.0 | 77.1
| GIH | 2.0 | 21.8 | 76.2
| LWK | 0.0 | 10.0 | 90.0
| MEX | 3.4 | 19.0 | 77.6
| MKK | 0.0 | 8.3 | 91.7
| TSI | 6.9 | 44.1 | 49.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=21298289
|Title=Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease
|OA=1
}}

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