{{Rsnum
|rsid=34716011
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBB
|position=5226974
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=34716011
|variant=0313
}}

{{ClinVar
|rsid=34716011
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=5248204
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000601000102110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5248204C>T
|CLNORIGIN=1
|CLNSIG=1
|Tags=RV;PM;PMC;S3D;SLO;NSN;REF;GNO;OTHERKG;LSD;OM
|CLNSRC=GTR; HBVAR
|CLNSRCID=GTR000500319; 793
}}

{{PMID Auto
|PMID=1428946
|Title=Hb Shelby [alpha 2 beta 2(131)(H9)Gln----Lys]-beta zero-thalassemia [codon 15 (TGG----TGA)] identified by DNA sequencing.
}}

{{PMID Auto
|PMID=1581247
|Title=A novel beta zero-thalassaemia mutation (codon 15, TGG----TGA) is prevalent in a population of central Portugal.
}}

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