{{Rsnum
|rsid=267607298
|Chromosome=11
|position=5226775
|Orientation=minus
|geno1=(-;-)
|geno2=(-;CC)
|geno3=(CC;CC)
|Gene=HBB
|Gene_s=HBB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=minus
}}{{ClinVar
|ALT=T
|CHROM=11
|CLNACC=RCV000016817.24
|CLNALLE=1
|CLNDBN=beta Thalassemia
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1426:C0005283:613985:848:65959000
|CLNHGVS=NC_000011.9:g.5248005_5248006delGG
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=844; 141900.0463
|Disease=beta Thalassemia
|FwdREF=CC
|GENEINFO=HBB:3043
|GENE_ID=3043
|GENE_NAME=HBB
|REF=TGG
|RSPOS=5248003
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050368000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=267607298
}}{{PMID Auto
|PMID=8682512
|Title=Beta-thalassaemia in indigenous Belgian families: identification of a novel mutation.
}}