{{Rsnum
|rsid=33943001
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBB
|position=5226800
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33943001
|variant=0356
}}
{{omim
|id=141900
|rsnum=33943001
|variant=0418
}}{{ClinVar
|rsid=33943001
|Reversed=1
|FwdREF=G
|FwdALT=A,C
|REF=C
|ALT=G,T
|RSPOS=5248030
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000011.9:g.5248030C>T
|CLNORIGIN=1
|CLNSRCID=
NBK1426; 33943001; 141900.0356
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000016704.24
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDBN=beta0^ Thalassemia
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0271980:86715000
|CLNSRC=GeneReviews; NCBI curation; OMIM Allelic Variant
|Disease=beta0^ Thalassemia
}}{{PMID Auto
|PMID=2200760
|Title=Beta-thalassemia in Turkey.
}}

{{PMID Auto
|PMID=2283297
|Title=A new beta-thalassemia mutation produced by a single nucleotide substitution in the conserved dinucleotide sequence of the IVS-I consensus acceptor site (AG----AA).
}}

{{PMID Auto
|PMID=1517108
|Title=Two beta-thalassemia mutations in Japan: codon 121 (GAA----TAA) and IVS-I-130 (G----C).
}}