{{Rsnum
|rsid=12073837
|Chromosome=1
|position=220836863
|Orientation=plus
|GMAF=0.258
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HLX-AS1
|Gene_s=HLX-AS1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 52.2 | 38.1 | 9.7
| HCB | 46.7 | 48.9 | 4.4
| JPT | 42.5 | 45.1 | 12.4
| YRI | 76.2 | 23.1 | 0.7
| ASW | 82.5 | 15.8 | 1.8
| CHB | 46.7 | 48.9 | 4.4
| CHD | 55.6 | 33.3 | 11.1
| GIH | 66.3 | 32.7 | 1.0
| LWK | 79.8 | 19.3 | 0.9
| MEX | 41.4 | 46.6 | 12.1
| MKK | 72.4 | 24.4 | 3.2
| TSI | 65.7 | 27.5 | 6.9
| 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=T
|Pval=0.000002
|OR=1.3900
|ORtxt=[0.82-1.96] unit increase
}}

{{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}}