{{Rsnum
|rsid=10128556
|Gene=HBBP1
|Chromosome=11
|position=5242453
|Orientation=plus
|GMAF=0.2011
|Gene_s=HBBP1
|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 | 46.2 | 49.2 | 4.6
| HCB | 66.7 | 31.1 | 2.2
| JPT | 71.1 | 28.9 | 0.0
| YRI | 87.3 | 11.1 | 1.6
| ASW | 0.0 | 0.0 | 0.0
| CHB | 66.7 | 31.1 | 2.2
| 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
}}[[Persistant Fetal Hemoglobin]]

{{PMID Auto
|PMID=20353593
|Title=Genetic modifiers of Hb E/beta0 thalassemia identified by a two-stage genome-wide association study.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}