{{Rsnum
|rsid=33956879
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=HBB
|position=5226928
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33956879
|variant=0349
}}
{{omim
|id=141900
|rsnum=33956879
|variant=0350
}}
{{omim
|id=141900
|rsnum=33956879
|variant=0392
}}

{{ClinVar
|rsid=33956879
|Reversed=1
|FwdREF=T
|FwdALT=A,C,G
|REF=A
|ALT=C,G,T
|RSPOS=5248158
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050168000000000402110104
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000011.9:g.5248158A>G
|CLNSRC=GTR; HBVAR
|CLNORIGIN=1
|CLNSRCID=
GTR000500319; 820
|CLNSIG=5
|CLNCUI=
|CLNDBN=beta Thalassemia
|Disease=beta Thalassemia
|CLNACC=
RCV000030003.1
|Tags=RV;PM;PMC;SLO;HD;OTHERKG;LSD;OM;NOV
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1426:C0005283:613985:848:65959000
}}

{{PMID|2393712}} A new mutation at IVS1 nt 2(T----A), in beta-thalassemia from Algeria.

{{PMID|2917118}} Severe Hb S-beta zero-thalassaemia with a T----C substitution in the donor splice site of the first intron of the beta-globin gene.

{{PMID|8037197}} An African origin for an "American black" beta zero-thalassemia mutation?

{{PMID|14576320|OA=1
}} Intrinsic differences between authentic and cryptic 5' splice sites.

{{PMID|15108284}} Real-time PCR for single-cell genotyping in sickle cell and thalassemia syndromes as a rapid, accurate, reliable, and widely applicable protocol for preimplantation genetic diagnosis.

{{PMID|20406103}} Mutation analysis of the HBB gene in selected Bangladeshi beta-thalassemic individuals: presence of rare mutations.

{{PMID Auto
|PMID=3422218
|Title=The peculiar spectrum of beta-thalassemia genes in Tunisia.
}}

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