{{Rsnum
|rsid=34598529
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBB
|position=5227100
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=34598529
|variant=0379
}}

{{ClinVar
|rsid=34598529
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=5248330
|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.5248330T>C
|CLNSRC=GTR; GeneReviews; HBVAR; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=GTR000167610; GTR000500319; NBK1426; 767; 141900.0379
|CLNSIG=5
|CLNCUI=C0039730
|CLNDBN=Beta-plus-thalassemia; alpha Thalassemia; Beta thalassemia intermedia
|Disease=Beta-plus-thalassemia; alpha Thalassemia; Beta thalassemia intermedia
|CLNACC=RCV000016727.21; RCV000020326.1; RCV000029961.1
|Tags=RV;PM;PMC;SLO;HD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:SNOMED_CT
|CLNDSDBID=NBK1426:NBK1435:C0002312:604131:846:68913001; C0472767:191189009
}}

{{PMID Auto
|PMID=1698102
|Title=Observations on the levels of Hb A2 in patients with different beta-thalassemia mutations and a delta chain variant.
}}

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

{{PMID Auto
|PMID=2460127
|Title=Hb S(C)-beta+-thalassaemia: different mutations are associated with different levels of normal Hb A.
}}

{{PMID Auto
|PMID=3799593
|Title=Clinical and molecular correlations in the sickle/beta+-thalassemia syndrome.
}}

{{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 v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}