{{Rsnum
|rsid=33941377
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HBB
|position=5227158
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33941377
|variant=0374
}}{{ClinVar
|rsid=33941377
|Reversed=1
|FwdREF=C
|FwdALT=A,G,T
|REF=G
|ALT=A,C,T
|RSPOS=5248388
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050168000000000002110104
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000011.9:g.5248388G>A; NC_000011.9:g.5248388G>C; NC_000011.9:g.5248388G>T
|CLNORIGIN=1
|CLNSRCID=
GTR000500319; 758; 141900.0374; 757
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000029952.1; RCV000016722.24; RCV000029951.1; RCV000029950.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM;NOV
|CLNDBN=Beta thalassemia intermedia; Beta-plus-thalassemia
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0472767:191189009
|CLNSRC=GTR; HBVAR; OMIM Allelic Variant
|Disease=Beta thalassemia intermedia; Beta-plus-thalassemia
}}{{PMID Auto
|PMID=1428943
|Title=The -87 (C----A) beta(+)-thalassemia mutation in a black family.
}}

{{PMID Auto
|PMID=2375912
|Title=The homozygous state for the -87 C----G beta + thalassaemia.
}}

{{PMID Auto
|PMID=2446680
|Title=Mild and severe beta-thalassemia among homozygotes from Turkey: identification of the types by hybridization of amplified DNA with synthetic probes.
}}

{{PMID Auto
|PMID=6188062
|Title=Specific transcription and RNA splicing defects in five cloned beta-thalassaemia genes.
}}

{{PMID Auto
|PMID=7507641
|Title=Mild beta+(-87)-thalassemia CACCC box mutation is associated with elevated fetal hemoglobin expression in cis.
}}

{{PMID Auto
|PMID=7655036
|Title=HLA-DR frequency in Turkish aplastic anemia patients and the impact of HLA-DR2 positivity in response rate in patients receiving immunosuppressive therapy.
}}

{{PMID Auto
|PMID=2018842
|Title=Thalassemia intermedia: moderate reduction of beta globin gene transcriptional activity by a novel mutation of the proximal CACCC promoter element.
}}