{{Rsnum
|rsid=2445284
|Chromosome=11
|position=5008473
|Orientation=plus
|GMAF=0.4913
|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 | 19.5 | 46.0 | 34.5
| HCB | 54.0 | 40.1 | 5.8
| JPT | 63.1 | 29.7 | 7.2
| YRI | 6.2 | 37.2 | 56.6
| ASW | 7.0 | 56.1 | 36.8
| CHB | 54.0 | 40.1 | 5.8
| CHD | 60.6 | 34.9 | 4.6
| GIH | 19.8 | 38.6 | 41.6
| LWK | 0.0 | 0.0 | 0.0
| MEX | 33.3 | 36.8 | 29.8
| MKK | 5.9 | 46.4 | 47.7
| TSI | 18.8 | 50.5 | 30.7
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23406172
  |Trait=Sickle cell anemia (haemolysis)
  |Title=Genetic determinants of haemolysis in sickle cell anaemia.
  |RiskAllele=G
  |Pval=1E-29
  |OR=.82
  |ORtxt=[0.68-0.96] 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}}