{{Rsnum
|rsid=34750035
|Chromosome=11
|Orientation=minus
|geno1=(-;-)
|geno2=(-;AG)
|geno3=(AG;AG)
|Gene=HBB
|position=5226572
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=34750035
|variant=0426
}}

{{ClinVar
|rsid=34750035
|Reversed=1
|FwdREF=AG
|FwdALT=
|REF=ACT
|ALT=A
|RSPOS=5247801
|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.5247802_5247803delCT
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016779.24
|CLNDBN=Beta-thalassemia intermedia, dominant
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=887; 141900.0426
|Disease=Beta-thalassemia intermedia
}}

{{PMID Auto
|PMID=1634236
|Title=Novel promoter and splice junction defects add to the genetic, clinical or geographic heterogeneity of beta-thalassaemia in the Portuguese population.
}}

{{on chip | 23andMe v3}}