{{Rsnum
|rsid=281864901
|Chromosome=11
|position=5226662
|Orientation=minus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=HBB
|Gene_s=HBB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=minus
}}{{ClinVar
|ALT=A
|CHROM=11
|CLNACC=RCV000016676.24
|CLNALLE=1
|CLNDBN=beta0^ Thalassemia
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0271980:86715000
|CLNHGVS=NC_000011.9:g.5247892delG
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=874; 141900.0330
|Disease=beta0^ Thalassemia
|FwdREF=C
|REF=AG
|RSPOS=5247891
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD
|VC=DIV
|VP=0x050368000000000002100200
|WGT=0
|dbSNPBuildID=137
|rsid=281864901
|GENEINFO=HBB:3043
|GENE_ID=3043
|GENE_NAME=HBB
}}{{PMID Auto
|PMID=7759073
|Title=The great heterogeneity of thalassemia molecular defects in Sicily.
}}