{{Rsnum
|rsid=33969727
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBB
|position=5226737
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33969727
|variant=0298
}}{{ClinVar
|rsid=33969727
|Reversed=1
|FwdREF=C
|FwdALT=A,G
|REF=G
|ALT=C,T
|RSPOS=5247967
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5247967G>C
|CLNORIGIN=1
|CLNSIG=255
|CLNCUI=
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016629.1
|CLNDBN=HEMOGLOBIN WILLAMETTE
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=332; 141900.0298
|Disease=HEMOGLOBIN WILLAMETTE
}}{{PMID Auto
|PMID=6590550
|Title=A second family with hemoglobin Willamette.
}}

{{PMID Auto
|PMID=6841127
|Title=Oxygen equilibrium studies of Hb Willamette alpha 2 beta (2)51(D2)Pro leads to Arg.
}}

{{PMID Auto
|PMID=9547908
|Title=The effect of an unusual haemoglobin variant (beta 51Pro-->His) on haemoglobin A1c measurement.
}}

{{PMID Auto
|PMID=11482884
|Title=Rapid identification of hemoglobin variants by electrospray ionization mass spectrometry.
}}