{{Rsnum
|rsid=33930702
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBB
|position=5227019
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33930702
|variant=0430
}}{{ClinVar
|rsid=33930702
|Reversed=1
|FwdREF=G
|FwdALT=A,C,T
|REF=C
|ALT=A,G,T
|RSPOS=5248249
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110104
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=3
|CLNHGVS=NC_000011.9:g.5248249C>T
|CLNORIGIN=1
|CLNSIG=5
|CLNCUI=
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNACC=RCV000016783.24
|CLNDBN=beta0^ Thalassemia
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0271980:86715000
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141900.0430
|Disease=beta0^ Thalassemia
}}{{PMID Auto
|PMID=1301952
|Title=A novel beta-thalassemia mutation (G-->A) at the initiation codon of the beta-globin gene.
}}

{{PMID Auto
|PMID=7864023
|Title=Initiation codon mutation (ATG --> ATA) of the beta-globin gene causing beta-thalassemia in a Swedish family.
}}

{{PMID Auto
|PMID=9101288
|Title=beta-thalassemia mutations in Japanese and Koreans.
}}

{{PMID Auto
|PMID=8718703
|Title=Molecular analyses of beta-thalassemia in Iran.
}}