{{Rsnum
|rsid=80356820
|Chromosome=11
|Orientation=minus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=HBB
|Gene_s=HBB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|position=5226757
}}{{ClinVar
|ALT=A
|CHROM=11
|CLNACC=RCV000016671.24; RCV000020329.1
|CLNALLE=1
|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
|CLNHGVS=NC_000011.9:g.5247987delG
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GTR; GeneReviews; HBVAR; OMIM Allelic Variant
|CLNSRCID=GTR000500319; NBK1426; 854; 141900.0324
|Disease=beta0^ Thalassemia; alpha Thalassemia
|FwdREF=C
|GENEINFO=HBB:3043
|GENE_ID=3043
|GENE_NAME=HBB
|REF=AG
|RSPOS=5247986
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050368000000000002110200
|WGT=0
|dbSNPBuildID=131
|rsid=80356820
}}{{PMID Auto
|PMID=1986379
|Title=Evolution of a genetic disease in an ethnic isolate: beta-thalassemia in the Jews of Kurdistan.
|OA=1
}}