{{Rsnum
|rsid=33931746
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBB
|position=5227099
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33931746
|variant=0380
}}
{{omim
|id=141900
|rsnum=33931746
|variant=0381
}}

{{ClinVar
|rsid=33931746
|Reversed=1
|FwdREF=A
|FwdALT=C,G
|REF=T
|ALT=C,G
|RSPOS=5248329
|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; 2
|CLNHGVS=NC_000011.9:g.5248329T>C; NC_000011.9:g.5248329T>G
|CLNORIGIN=0; 1
|CLNSRCID=
GTR000500319; NBK1426; 141900.0381; 141900.0380
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000016729.24; RCV000020325.1; RCV000029960.1; RCV000016728.21
|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=GTR; GeneReviews; OMIM Allelic Variant
|Disease=Beta-plus-thalassemia; alpha Thalassemia; beta Thalassemia
}}

{{PMID|19087310|OA=1
}} Microarray-based estimation of SNP allele-frequency in pooled DNA using the Langmuir kinetic model.

{{PMID Auto
|PMID=7076659
|Title=beta-Thalassemia in a Kurdish Jew. Single base changes in the T-A-T-A box.
}}

{{PMID Auto
|PMID=6308558
|Title=ATA box transcription mutation in beta-thalassemia.
|OA=1
}}

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