{{Rsnum
|rsid=33994806
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HBB
|position=5227157
|Gene_s=HBB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=33994806
|Reversed=1
|FwdREF=C
|FwdALT=A,G
|REF=G
|ALT=C,T
|RSPOS=5248387
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050168000000000402110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5248387G>C
|CLNORIGIN=0
|CLNSRCID=
NBK1426; 141900.0375
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000016723.24; RCV000020323.1; RCV000029948.1
|Tags=RV;PM;PMC;SLO;HD;OTHERKG;LSD;OM
|CLNDBN=Beta-plus-thalassemia; alpha Thalassemia; beta Thalassemia
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1426:NBK1435:C0002312:604131:846:68913001; NBK1426:C0005283:613985:848:65959000
|CLNSRC=GeneReviews; OMIM Allelic Variant
|Disease=Beta-plus-thalassemia; alpha Thalassemia; beta Thalassemia
}}

{{PMID Auto
|PMID=1550780
|Title=Promoter mutations producing mild beta-thalassaemia in the Italian population.
}}

{{PMID Auto
|PMID=2197725
|Title=The thalassemia syndromes: molecular basis and prenatal diagnosis in 1990.
}}

{{PMID Auto
|PMID=2393018
|Title=The molecular basis of beta-thalassemia in Thailand: application to prenatal diagnosis.
|OA=1
}}

{{on chip | HumanOmni1Quad}}