{{Rsnum
|rsid=34999973
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBB
|position=5227161
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=34999973
|variant=0425
}}

{{ClinVar
|rsid=34999973
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=5248391
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5248391G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016778.24; RCV000029954.1
|CLNDBN=Beta-plus-thalassemia; beta Thalassemia
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1426:C0005283:613985:848:65959000
|CLNSRC=GTR; HBVAR; OMIM Allelic Variant
|CLNSRCID=GTR000500319; 754; 141900.0425
|Disease=Beta-plus-thalassemia; beta Thalassemia
}}

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