{{Rsnum
|rsid=33913413
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBB
|position=5225729
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33913413
|variant=0361
}}
{{omim
|id=141900
|rsnum=33913413
|variant=0416
}}{{ClinVar
|rsid=33913413
|Reversed=1
|FwdREF=C
|FwdALT=A,G
|REF=G
|ALT=C,T
|RSPOS=5246959
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050168000000000502110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000011.9:g.5246959G>T
|CLNSRC=GTR; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=
GTR000500319; 141900.0361
|CLNSIG=5
|CLNCUI=
|CLNDBN=Beta-plus-thalassemia; Beta thalassemia intermedia
|Disease=Beta-plus-thalassemia; Beta thalassemia intermedia
|CLNACC=
RCV000016709.24; RCV000029987.1
|Tags=RV;PM;PMC;SLO;HD;GNO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0472767:191189009
}}{{PMID Auto
|PMID=1917531
|Title=Beta-thalassemia, HB S-beta-thalassemia and sickle cell anemia among Tunisians.
}}

{{PMID Auto
|PMID=2200760
|Title=Beta-thalassemia in Turkey.
}}

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

{{PMID Auto
|PMID=2920213
|Title=Beta-thalassemia due to two novel nucleotide substitutions in consensus acceptor splice sequences of the beta-globin gene.
}}

{{PMID Auto
|PMID=9140720
|Title=A significant beta-thalassemia heterogeneity in the United Arab Emirates.
}}

{{PMID Auto
|PMID=20437613
|Title=Mutations of a country: a mutation review of single gene disorders in the United Arab Emirates (UAE).
}}{{PMID Auto
|PMID=1634368
|Title=Three beta-thalassemia mutations in the Japanese: IVS-II-1 (G----A), IVS-II-848 (C----G), and codon 90 (GAG----TAG).
}}