{{Rsnum
|rsid=7948471
|Gene=OR51B5
|Chromosome=11
|position=5450516
|Orientation=plus
|GMAF=0.4068
|Gene_s=OR51B5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 34.5 | 45.1 | 20.4
| HCB | 8.8 | 35.0 | 56.2
| JPT | 6.2 | 33.6 | 60.2
| YRI | 21.1 | 42.9 | 36.1
| ASW | 17.5 | 64.9 | 17.5
| CHB | 8.8 | 35.0 | 56.2
| CHD | 7.3 | 40.4 | 52.3
| GIH | 15.8 | 37.6 | 46.5
| LWK | 7.3 | 48.2 | 44.5
| MEX | 20.7 | 53.4 | 25.9
| MKK | 10.3 | 48.7 | 41.0
| TSI | 20.6 | 47.1 | 32.4
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23406172
  |Trait=Sickle cell anemia (haemolysis)
  |Title=Genetic determinants of haemolysis in sickle cell anaemia.
  |RiskAllele=A
  |Pval=3E-10
  |OR=.26
  |ORtxt=[0.18-0.34] unit decrease
  }}

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