{{Rsnum
|rsid=9838682
|Chromosome=3
|position=30349375
|Orientation=plus
|GMAF=0.4504
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=LOC101927995
|Gene_s=LOC101927995
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 16.7 | 45.0 | 38.3
| HCB | 17.4 | 43.9 | 38.6
| JPT | 17.5 | 45.0 | 37.5
| YRI | 44.8 | 45.5 | 9.7
| ASW | 33.3 | 47.4 | 19.3
| CHB | 17.4 | 43.9 | 38.6
| CHD | 12.0 | 44.4 | 43.5
| GIH | 8.2 | 46.9 | 44.9
| LWK | 46.4 | 44.5 | 9.1
| MEX | 0.0 | 0.0 | 0.0
| MKK | 38.3 | 49.4 | 12.3
| TSI | 19.0 | 48.0 | 33.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=19959123
|Title=Association of TGFBR2 polymorphism with risk of sudden cardiac arrest in patients with coronary artery disease
|OA=1
}}

{{PMID Auto
|PMID=19654303
|Title=Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}