{{Rsnum
|rsid=193922553
|Chromosome=11
|Orientation=minus
|geno1=(-;-)
|geno2=(-;A)
|geno3=(A;A)
|Gene=HBB
|position=5226691
|Gene_s=HBB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922553
|Reversed=1
|FwdREF=A
|FwdALT=
|REF=CT
|ALT=C
|RSPOS=5247920
|CHROM=11
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002100200
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5247921delT
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Beta thalassemia, dominant inclusion body type
|Disease=Beta thalassemia
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000029967.1
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1858990:603902:231226
|GENEINFO=HBB:3043
|GENE_ID=3043
|GENE_NAME=HBB
}}{{PMID Auto
|PMID=20532507
|Title=A novel frameshift mutation at codon 66 (HBB:c.del201A) in the beta-globin gene leads to beta-thalassemia.
}}