{{Rsnum
|rsid=33916412
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBB
|position=5226936
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33916412
|variant=0093
}}
{{omim
|id=141900
|rsnum=33916412
|variant=0268
}}
{{omim
|id=141900
|rsnum=33916412
|variant=0402
}}

{{ClinVar
|rsid=33916412
|Reversed=1
|FwdREF=T
|FwdALT=A,C,G
|REF=A
|ALT=C,G,T
|RSPOS=5248166
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000402110104
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000011.9:g.5248166A>C; NC_000011.9:g.5248166A>G; NC_000011.9:g.5248166A>T
|CLNORIGIN=1
|CLNSRCID=
286; 141900.0402; 285; 141900.0093; 284; 141900.0268
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016751.1; RCV000016362.1; RCV000016363.1; RCV000016611.1; RCV000016612.24
|Tags=RV;PM;PMC;S3D;SLO;HD;OTHERKG;LSD;OM;NOV
|CLNDBN=HEMOGLOBIN CHESTERFIELD; HEMOGLOBIN GENOVA; HEMOGLOBIN HYOGO; HEMOGLOBIN ST. LOUIS; Heinz body hemolytic anemia
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN CHESTERFIELD; HEMOGLOBIN GENOVA; HEMOGLOBIN HYOGO; HEMOGLOBIN ST. LOUIS; Heinz body hemolytic anemia
}}

{{PMID Auto
|PMID=186485
|Title=Functional and physicochemical studies of hemoglobin St. Louis beta 28 (B10) Leu replaced by Gln: a variant with ferric beta heme iron.
|OA=1
}}

{{PMID Auto
|PMID=3557999
|Title=Hb Saint Louis or alpha 2 beta 2(28)(B10)Leu----Gln in a Czechoslovakian male.
}}

{{PMID Auto
|PMID=4722493
|Title=Haemoglobin Saint Louis beta28 (B10) leucine leads to glutamine. A new unstable haemoglobin only present in a ferri form.
}}

{{PMID Auto
|PMID=2105568
|Title=A case of the unstable Hb Genova (beta 28 Leu----Pro) in an Arab child associated with severe haemolytic anaemia and growth retardation.
}}

{{PMID Auto
|PMID=4685078
|Title=A new case of hemoglobin Genova 2 2 28(B10) Leu leads to Pro. Further studies on the mechanism of instability and defective synthesis.
}}

{{PMID Auto
|PMID=6054966
|Title=Haemoglobin Genova: beta-28 (B10) leucine replaced by proline.
}}

{{PMID Auto
|PMID=1675132
|Title=Hemoglobin Chesterfield (beta 28 Leu----Arg) produces the phenotype of inclusion body beta thalassemia.
}}

{{on chip | HumanOmni1Quad}}