{{Rsnum
|rsid=80356821
|Chromosome=11
|Orientation=minus
|geno1=(-;-)
|geno2=(-;TTCT)
|geno3=(TTCT;TTCT)
|Gene=HBB
|Gene_s=HBB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|position=5226765
}}{{ClinVar
|ALT=A
|CHROM=11
|CLNACC=RCV000016673.24; RCV000020328.1
|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.5247995_5247998delAGAA
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=GTR; GeneReviews; HBVAR; OMIM Allelic Variant
|CLNSRCID=GTR000500319; NBK1426; 849; 141900.0326
|Disease=beta0^ Thalassemia; alpha Thalassemia
|FwdREF=TCTT
|GENEINFO=HBB:3043
|GENE_ID=3043
|GENE_NAME=HBB
|REF=AAGAA
|RSPOS=5247994
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050360000000000002110200
|WGT=0
|dbSNPBuildID=131
|rsid=80356821
}}