{{Rsnum
|rsid=33985472
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBB
|position=5225485
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33985472
|variant=0383
}}

{{ClinVar
|rsid=33985472
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=5246715
|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.5246715T>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016731.21
|CLNDBN=Beta-plus-thalassemia
|CLNSRC=GTR; OMIM Allelic Variant
|CLNSRCID=GTR000500319; 141900.0383
|Disease=Beta-plus-thalassemia
}}

{{PMID Auto
|PMID=20808897
|Title=Disease-associated mutations that alter the RNA structural ensemble.
|OA=1
}}

{{PMID Auto
|PMID=1705411
|Title=Molecular studies of beta-thalassemia in Israel. Mutational analysis and expression studies.
}}

{{PMID Auto
|PMID=1986379
|Title=Evolution of a genetic disease in an ethnic isolate: beta-thalassemia in the Jews of Kurdistan.
|OA=1
}}

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