{{Rsnum
|rsid=17135859
|Chromosome=5
|position=113660957
|Orientation=plus
|GMAF=0.1322
|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 | 1.8 | 33.6 | 64.6
| HCB | 0.0 | 8.0 | 92.0
| JPT | 0.0 | 4.4 | 95.6
| YRI | 2.7 | 30.6 | 66.7
| ASW | 7.0 | 29.8 | 63.2
| CHB | 0.0 | 8.0 | 92.0
| CHD | 0.9 | 4.6 | 94.5
| GIH | 5.9 | 24.8 | 69.3
| LWK | 2.7 | 27.3 | 70.0
| MEX | 0.0 | 22.4 | 77.6
| MKK | 1.3 | 23.1 | 75.6
| TSI | 2.9 | 17.6 | 79.4
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21326311
|Trait=None
|Title=Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients
|RiskAllele=C
|Pval=0.000008
|OR=0.9700
|ORtxt=[0.54-1.40] unit increase
}}

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