{{Rsnum
|rsid=4671393
|Gene=BCL11A
|Chromosome=2
|position=60493816
|Orientation=plus
|GMAF=0.213
|Gene_s=BCL11A,LOC100286932
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 23.1 | 76.9
| HCB | 11.1 | 35.6 | 53.3
| JPT | 0.0 | 35.6 | 64.4
| YRI | 1.6 | 46.0 | 52.4
| ASW | 0.0 | 0.0 | 0.0
| CHB | 11.1 | 35.6 | 53.3
| 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
}}{{omim
|desc=FETAL HEMOGLOBIN QUANTITATIVE TRAIT LOCUS 5; HBFQTL5
|id=142335
|rsnum=4671393
}}

{{omim
|desc=SICKLE CELL ANEMIA
|id=603903
|rsnum=4671393
}}
{{PMID Auto
|PMID=20472475
|Title=The XmnI (G)gamma polymorphism influences hemoglobin F synthesis contrary to BCL11A and HBS1L-MYB SNPs in a cohort of 57 beta-thalassemia intermedia patients
}}{{PMID|18667698|OA=1
}} DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease.

{{PMID|18695233|OA=1
}} Genetic complexity in sickle cell disease.

{{PMID|19966804|OA=1
}} Geographical genomics of human leukocyte gene expression variation in southern Morocco.

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

{{PMID|22258351}} Analysis of rs4671393 polymorphism in hemoglobin E/beta-thalassemia major in Guangxi Province of China.