{{Rsnum
|rsid=766432
|Gene=BCL11A
|Chromosome=2
|position=60492835
|Orientation=plus
|GMAF=0.2153
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=BCL11A
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 69.9 | 27.4 | 2.7
| HCB | 52.9 | 39.0 | 8.1
| JPT | 61.9 | 31.0 | 7.1
| YRI | 54.8 | 42.5 | 2.7
| ASW | 57.9 | 36.8 | 5.3
| CHB | 52.9 | 39.0 | 8.1
| CHD | 56.0 | 36.7 | 7.3
| GIH | 78.2 | 20.8 | 1.0
| LWK | 50.5 | 37.6 | 11.9
| MEX | 48.3 | 46.6 | 5.2
| MKK | 32.3 | 49.7 | 18.1
| TSI | 62.7 | 34.3 | 2.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19924444
|Trait=Beta thalassemia/hemoglobin E disease
|Title=A genome-wide association identified the common genetic variants influence disease severity in beta(0)-thalassemia/hemoglobin E
|RiskAllele=
|Pval=1E-10
|OR=2.80
|ORtxt=[2.04-3.84]
}}

{{PMID Auto
|PMID=20018918
|Title=Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster
|OA=1
}}

{{PMID Auto GWAS
|PMID=20183929
|Trait=Beta thalassemia/hemoglobin E disease
|Title=A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E.
|RiskAllele=
|Pval=1E-10
|OR=2.8000
|ORtxt=[2.04-3.84]
}}

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

{{PMID Auto
|PMID=21326311
|Title=Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients.
}}

{{PMID Auto
|PMID=22686296
|Title=The XmnI and BCL11A Single Nucleotide Polymorphisms May Help Predict Hydroxyurea Response in Iranian beta-Thalassemia Patients.
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs766432
|overall_frequency_n=100
|overall_frequency_d=128
|overall_frequency=0.78125
|n_genomes=52
|n_genomes_annotated=0
|n_haplomes=85
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=2
|webscore=N
}}

{{PMID Auto GWAS
  |PMID=23406172
  |Trait=Sickle cell anemia (haemolysis)
  |Title=Genetic determinants of haemolysis in sickle cell anaemia.
  |RiskAllele=
  |Pval=9E-7
  |OR=.22
  |ORtxt=NR unit increase
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}