{{Rsnum
|rsid=9483788
|Chromosome=6
|position=135114363
|Orientation=plus
|GMAF=0.2034
|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 | 4.7 | 25.0 | 70.3
| HCB | 13.6 | 34.1 | 52.3
| JPT | 14.0 | 41.9 | 44.2
| YRI | 0.0 | 11.3 | 88.7
| ASW | 0.0 | 0.0 | 0.0
| CHB | 13.6 | 34.1 | 52.3
| 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=19862010
|Trait=Hematocrit
|Title=Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
|RiskAllele=C
|Pval=3E-15
|OR=0.22
|ORtxt=[0.16-0.28] % increase
|OA=1
}}

{{PMID Auto
|PMID=17592125
|Title=Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults.
|OA=1
}}

{{PMID Auto
|PMID=20401335
|Title=Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs9483788
|overall_frequency_n=23
|overall_frequency_d=128
|overall_frequency=0.179688
|n_genomes=18
|n_genomes_annotated=0
|n_haplomes=20
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}