{{Rsnum
|rsid=33944208
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HBB
|position=5227159
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33944208
|variant=0372
}}
{{omim
|id=141900
|rsnum=33944208
|variant=0373
}}

{{ClinVar
|rsid=33944208
|Reversed=1
|FwdREF=C
|FwdALT=A,G,T
|REF=G
|ALT=A,C,T
|RSPOS=5248389
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050168000000000402110104
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5248389G>A
|CLNORIGIN=1
|CLNSRCID=
GTR000167610; GTR000500319; NBK1426; 756; 141900.0372
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000016718.24; RCV000020324.1; RCV000029953.1
|Tags=RV;PM;PMC;SLO;HD;OTHERKG;LSD;OM;NOV
|CLNDBN=Beta-plus-thalassemia; alpha Thalassemia; Beta thalassemia intermedia
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:SNOMED_CT
|CLNDSDBID=NBK1426:NBK1435:C0002312:604131:846:68913001; C0472767:191189009
|CLNSRC=GTR; GeneReviews; HBVAR; OMIM Allelic Variant
|Disease=Beta-plus-thalassemia; alpha Thalassemia; Beta thalassemia intermedia
}}

{{PMID Auto
|PMID=1986379
|Title=Evolution of a genetic disease in an ethnic isolate: beta-thalassemia in the Jews of Kurdistan.
|OA=1
}}

{{PMID Auto
|PMID=1384315
|Title=Black beta-thalassemia homozygotes with specific sequence variations in the 5' hypersensitive site-2 of the locus control region have high levels of fetal hemoglobin.
}}

{{PMID Auto
|PMID=2458145
|Title=Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States.
}}

{{PMID Auto
|PMID=3462712
|Title=On the origin and spread of beta-thalassemia: recurrent observation of four mutations in different ethnic groups.
|OA=1
}}

{{PMID Auto
|PMID=6086605
|Title=Base substitution at position -88 in a beta-thalassemic globin gene. Further evidence for the role of distal promoter element ACACCC.
}}

{{PMID Auto
|PMID=9401495
|Title=Levels of Hb A2 in heterozygotes and homozygotes for beta-thalassemia mutations: influence of mutations in the CACCC and ATAAA motifs of the beta-globin gene promoter.
}}

{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}