{{Rsnum
|rsid=33913712
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBB
|position=5226621
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33913712
|variant=0003
}}
{{omim
|id=141900
|rsnum=33913712
|variant=0415
}}
{{omim
|id=141900
|rsnum=33913712
|variant=0521
}}{{ClinVar
|rsid=33913712
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=5247851
|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.5247851C>A; NC_000011.9:g.5247851C>T
|CLNORIGIN=1
|CLNSRCID=
141900.0415; 424; 141900.0003; 141900.0521
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016766.24; RCV000016244.1; RCV000016877.1
|Tags=RV;PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNDBN=beta0^ Thalassemia; HEMOGLOBIN AGENOGI; HEMOGLOBIN S (CAMEROON)
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0271980:86715000
|CLNSRC=OMIM Allelic Variant; HBVAR
|Disease=beta0^ Thalassemia; HEMOGLOBIN AGENOGI; HEMOGLOBIN S (CAMEROON)
}}{{PMID Auto
|PMID=2079434
|Title=Hb Agenogi [beta 90(F6)Glu----Lys] and beta zero-thalassemia in a Sicilian family.
}}

{{PMID Auto
|PMID=5416123
|Title=Studies on the function of abnormal hemoglobins. II. Oxygen equilibrium of abnormal hemoglobins: Shimonoseki, Ube II, Hikari, Gifu, and Agenogi.
}}

{{PMID Auto
|PMID=5972415
|Title=Hemoglobin agenogi (alpha 2 beta 2-90Lys), a slow-moving hemoglobin of a Japanese family resembling Hb-E.
}}

{{PMID Auto
|PMID=9785927
|Title=Hemoglobin Agenogi [beta 90 (F6) Glu-->Lys] found in Piedmont. Case report.
}}

{{PMID Auto
|PMID=12144066
|Title=Hb Agenogi [P90(F6)Glu-->Lys] in an Argentinean girl.
}}

{{PMID Auto
|PMID=1634368
|Title=Three beta-thalassemia mutations in the Japanese: IVS-II-1 (G----A), IVS-II-848 (C----G), and codon 90 (GAG----TAG).
}}

{{PMID Auto
|PMID=2310691
|Title=Molecular heterogeneity of beta-thalassaemia in the Japanese: identification of two novel mutations.
}}