{{Rsnum
|rsid=33969400
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBB
|position=5226714
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33969400
|variant=0115
}}{{ClinVar
|rsid=33969400
|Reversed=1
|FwdREF=A
|FwdALT=G,T
|REF=T
|ALT=A,C
|RSPOS=5247944
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000102110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000011.9:g.5247944T>C
|CLNORIGIN=1
|CLNSIG=255
|CLNCUI=
|Tags=RV;PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNACC=RCV000016389.1
|CLNDBN=HEMOGLOBIN I (HIGH WYCOMBE)
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141900.0115
|Disease=HEMOGLOBIN I (HIGH WYCOMBE)
}}{{PMID Auto
|PMID=3583766
|Title=Hemoglobin I High Wycombe in an Australian family.
}}

{{PMID Auto
|PMID=10870888
|Title=Hb I-high Wycombe [beta59(E3)Lys-->Glu]: the first instance in Japan.
}}

{{PMID Auto
|PMID=12908806
|Title=Identification of a new beta-thalassemia nonsense mutation [codon 59 (AAG-->TAG)].
}}