{{Rsnum
|rsid=63750532
|Chromosome=11
|Orientation=minus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=HBB
|position=5226780
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=63750532
|variant=0341
}}{{ClinVar
|rsid=63750532
|Reversed=1
|FwdREF=T
|FwdALT=
|REF=CA
|ALT=C
|RSPOS=5248009
|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.5248010delA
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016688.24
|CLNDBN=beta0^ Thalassemia
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0271980:86715000
|CLNSRC=GTR; HBVAR; OMIM Allelic Variant
|CLNSRCID=GTR000500319; 840; 141900.0331; 141900.0341
|Disease=beta0^ Thalassemia
}}{{PMID Auto
|PMID=2197725
|Title=The thalassemia syndromes: molecular basis and prenatal diagnosis in 1990.
}}

{{PMID Auto
|PMID=1986379
|Title=Evolution of a genetic disease in an ethnic isolate: beta-thalassemia in the Jews of Kurdistan.
|OA=1
}}