{{Rsnum
|rsid=63751208
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBB
|position=5227172
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=63751208
|variant=0370
}}

{{ClinVar
|rsid=63751208
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=5248402
|CHROM=11
|dbSNPBuildID=137
|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.5248402G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016719.24
|CLNDBN=Beta-plus-thalassemia
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=649; 141900.0370
|Disease=Beta-plus-thalassemia
}}

{{PMID Auto
|PMID=2713503
|Title=A C----T substitution at nt--101 in a conserved DNA sequence of the promotor region of the beta-globin gene is associated with "silent" beta-thalassemia.
}}

{{PMID Auto
|PMID=2346726
|Title=The C-T substitution in the distal CACCC box of the beta-globin gene promoter is a common cause of silent beta thalassaemia in the Italian population.
}}

{{PMID Auto
|PMID=7909640
|Title=Binding of nuclear factors to the proximal and distal CACCC motifs of the beta-globin gene promoter: implications for the -101 (C-->T) 'silent' beta-thalassemia mutation.
}}

{{PMID Auto
|PMID=8172199
|Title=Genotype of subjects with borderline hemoglobin A2 levels: implication for beta-thalassemia carrier screening.
}}

{{PMID Auto
|PMID=8980256
|Title=Genetic analysis of beta-thalassemia intermedia in Israel: diversity of mechanisms and unpredictability of phenotype.
}}

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