{{Rsnum
|rsid=34883338
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBB
|position=5227163
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=34883338
|variant=0371
}}

{{ClinVar
|rsid=34883338
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=5248393
|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.5248393G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016720.24
|CLNDBN=Beta-plus-thalassemia
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=752; 141900.0371
|Disease=Beta-plus-thalassemia
}}

{{PMID Auto
|PMID=2197725
|Title=The thalassemia syndromes: molecular basis and prenatal diagnosis in 1990.
}}

{{PMID Auto
|PMID=7794779
|Title=A promoter mutation, C-->T at position -92, leading to silent beta-thalassaemia.
}}

{{PMID Auto
|PMID=8438884
|Title=A mild type of Hb S-beta(+)-thalassemia [-92(C-->T)] in a Sicilian family.
}}

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