{{Rsnum
|rsid=33910569
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HBB
|position=5225659
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33910569
|variant=0319
}}
{{omim
|id=141900
|rsnum=33910569
|variant=0448
}}{{ClinVar
|rsid=33910569
|Reversed=1
|FwdREF=A
|FwdALT=C,G
|REF=T
|ALT=C,G
|RSPOS=5246889
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000102110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000011.9:g.5246889T>C; NC_000011.9:g.5246889T>G
|CLNORIGIN=1
|CLNSRCID=
524; 141900.0448; 959; 141900.0319
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016802.1; RCV000016664.25; RCV000022611.24
|Tags=RV;PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNDBN=HEMOGLOBIN DIEPPE; Beta-Houston-thalassemia; BETA-PLUS-THALASSEMIA, DOMINANT
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN DIEPPE; Beta-Houston-thalassemia; BETA-PLUS-THALASSEMIA
}}{{PMID Auto
|PMID=1420507
|Title=Rapid molecular characterization of mutations leading to unstable hemoglobin beta-chain variants.
}}

{{PMID Auto
|PMID=1586746
|Title=Dominant thalassemia-like phenotypes associated with mutations in exon 3 of the beta-globin gene.
}}