{{Rsnum
|rsid=33969853
|Chromosome=11
|Orientation=minus
|geno1=(-;-)
|geno2=(-;A)
|geno3=(A;A)
|Gene=HBB
|position=5226675
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33969853
|variant=0328
}}
{{omim
|id=141900
|rsnum=33969853
|variant=0343
}}{{ClinVar
|rsid=33969853
|Reversed=1
|FwdREF=A
|FwdALT=AA,TA
|REF=T
|ALT=TA,TT
|RSPOS=5247905
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110200
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=DIV
|CLNALLE=2
|CLNHGVS=NC_000011.9:g.5247905_5247906insT
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016675.24
|CLNDBN=beta0^ Thalassemia
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0271980:86715000
|CLNSRC=GTR; HBVAR; OMIM Allelic Variant
|CLNSRCID=GTR000500319; 869; 141900.0328
|Disease=beta0^ Thalassemia
}}{{PMID Auto
|PMID=6585831
|Title=beta-Thalassemia in Chinese: use of in vivo RNA analysis and oligonucleotide hybridization in systematic characterization of molecular defects.
|OA=1
}}