{{Rsnum
|rsid=33974228
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBB
|position=5226988
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33974228
|variant=0099
}}
{{omim
|id=141900
|rsnum=33974228
|variant=0446
}}
{{omim
|id=141900
|rsnum=33974228
|variant=0507
}}{{ClinVar
|rsid=33974228
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=5248218
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000102110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000011.9:g.5248218C>A; NC_000011.9:g.5248218C>T
|CLNORIGIN=1
|CLNSRCID=
241; 141900.0446; 239; 141900.0099; 141900.0507
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016800.1; RCV000016370.1; RCV000016863.1
|Tags=RV;PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNDBN=HEMOGLOBIN WASHTENAW; HEMOGLOBIN HAMILTON; HEMOGLOBIN O (TIBESTI)
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN WASHTENAW; HEMOGLOBIN HAMILTON; HEMOGLOBIN O (TIBESTI)
}}{{PMID Auto
|PMID=1428944
|Title=Hb H disease in association with the silent beta chain variant Hb Hamilton or alpha 2 beta 2(11)(A8)Val----Ile.
}}

{{PMID Auto
|PMID=1610915
|Title=Identification of Hb Hamilton or beta 11(A8)Val----Ile gene by the polymerase chain reaction amplification technique.
}}

{{PMID Auto
|PMID=6695908
|Title=Hemoglobin Hamilton or alpha 2 beta 2 11(A8)Val leads to Ile: a silent beta-chain variant detected by Triton X-100 acid-urea polyacrylamide gel electrophoresis.
}}