{{Rsnum
|rsid=33971440
|Gene=HBB
|Chromosome=11
|position=5226929
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33971440
|variant=0346
}}
{{omim
|id=141900
|rsnum=33971440
|variant=0347
}}

{{ClinVar
|rsid=33971440
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=5248159
|CHROM=11
|GMAF=0.0005
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050168000000040416110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000011.9:g.5248159C>A; NC_000011.9:g.5248159C>T
|CLNORIGIN=1; 0
|CLNSRCID=
GTR000500319; 818; 141900.0347; NBK1426; 817; 141900.0346
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000016695.24; RCV000016694.24; RCV000020340.1
|Tags=RV;PM;PMC;SLO;VLD;HD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDBN=beta0^ Thalassemia; alpha Thalassemia
|CLNDSDB=MedGen:SNOMED_CT; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0271980:86715000; NBK1426:NBK1435:C0002312:604131:846:68913001
|CLNSRC=GTR; HBVAR; OMIM Allelic Variant; GeneReviews
|COMMON=0
|Disease=beta0^ Thalassemia; alpha Thalassemia
}}

{{PMID Auto
|PMID=1390250
|Title=The beta-thalassaemia mutations in the population of Cyprus.
}}

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

{{PMID Auto
|PMID=6280057
|Title=Linkage of beta-thalassaemia mutations and beta-globin gene polymorphisms with DNA polymorphisms in human beta-globin gene cluster.
}}

{{PMID Auto
|PMID=8602996
|Title=Beta-thalassaemia in south-western Spain: high frequency of G-->A (IVS I-1) mutation.
}}

{{PMID Auto
|PMID=6714226
|Title=Molecular characterization of seven beta-thalassemia mutations in Asian Indians.
|OA=1
}}

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