{{Rsnum
|rsid=34937014
|Chromosome=11
|Orientation=minus
|geno1=(-;-)
|geno2=(-;A)
|geno3=(A;A)
|Gene=HBB
|position=5226604
|Gene_s=HBB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=34937014
|Reversed=1
|FwdALT=A
|REF=C
|ALT=CT
|RSPOS=5247834
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002100200
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5247835dupT
|CLNSRC=GTR; HBVAR
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=beta Thalassemia
|Disease=beta Thalassemia
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD
|CLNACC=RCV000029975.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1426:C0005283:613985:848:65959000
|CLNSRCID=GTR000500319; 882
}}

{{PMID|1515453}} Identification of five rare mutations including a novel frameshift mutation causing beta zero-thalassemia in Thai patients with beta zero-thalassemia/hemoglobin E disease.

{{on chip | 23andMe v3}}