{{Rsnum
|rsid=34502690
|Chromosome=11
|Orientation=minus
|geno1=(-;-)
|geno2=(-;AGG)
|geno3=(AGG;AGG)
|Gene=HBB
|position=5225657
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=34502690
|variant=0320
}}

{{ClinVar
|rsid=34502690
|Reversed=1
|FwdREF=AGG
|FwdALT=
|REF=GCCT
|ALT=G
|RSPOS=5246886
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050168000000000002110200
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5246887_5246889delCCT
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016665.24
|CLNDBN=Beta-plus-thalassemia
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=962; 141900.0320
|Disease=Beta-plus-thalassemia
}}

{{PMID Auto
|PMID=2224139
|Title=Three-base deletion in exon 3 of the beta-globin gene produced a novel variant (beta gunma) with a thalassemia-like phenotype.
}}

{{PMID Auto
|PMID=2634667
|Title=Characterization of beta-thalassemia mutations among the Japanese.
}}

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

{{on chip | 23andMe v1}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}