{{Rsnum
|rsid=63750860
|Chromosome=11
|Orientation=minus
|geno1=(CCACA;CCACA)
|geno2=(CCACA;GCTG)
|geno3=(GCTG;GCTG)
|Gene=HBB
|position=5225654
|Gene_s=HBB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=63750860
|Reversed=1
|FwdREF=GCTG
|FwdALT=CCACA
|REF=GCAGC
|ALT=GTGTGG
|RSPOS=5246883
|CHROM=11
|dbSNPBuildID=137
|SSR=0
|SAO=1
|VP=0x050368000000000002110200
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5246884_5246887delCAGCinsTGTGG
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016876.24
|CLNDBN=Beta-thalassemia, dominant inclusion body type
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141900.0520
|Disease=Beta-thalassemia
}}

{{PMID Auto
|PMID=1971109
|Title=Molecular basis for dominantly inherited inclusion body beta-thalassemia.
|OA=1
}}

{{PMID Auto
|PMID=4351905
|Title=A genetically determined disorder with features both of thalassaemia and congenital dyserythropoietic anaemia.
}}

{{on chip | 23andMe v3}}