{{Rsnum
|rsid=172166
|Gene=OR2B8P
|Chromosome=6
|position=28053042
|Orientation=plus
|GMAF=0.2525
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 63.5 | 23.8 | 12.7
| HCB | 60.5 | 34.9 | 4.7
| JPT | 63.9 | 30.6 | 5.6
| YRI | 32.8 | 45.9 | 21.3
| ASW | 0.0 | 0.0 | 0.0
| CHB | 60.5 | 34.9 | 4.7
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23247143
  |Trait=Cardiac Troponin-T levels
  |Title=Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European americans and blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.
  |RiskAllele=C
  |Pval=5E-6
  |OR=.04
  |ORtxt=[0.04-0.06] ug/L decrease
  |OA=1
}}

{{on chip | HumanOmni1Quad}}