{{Rsnum
|rsid=33993568
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HBB
|position=5226629
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33993568
|variant=0062
}}
{{omim
|id=141900
|rsnum=33993568
|variant=0403
}}{{ClinVar
|rsid=33993568
|Reversed=1
|FwdREF=C
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=5247859
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000040102110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000011.9:g.5247859G>A; NC_000011.9:g.5247859G>T
|CLNORIGIN=1
|CLNSRCID=
418; 141900.0403; 416; 141900.0062
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016753.1; RCV000016754.1; RCV000016313.1
|Tags=RV;PM;PMC;S3D;SLO;VLD;GNO;OTHERKG;LSD;OM
|CLNDBN=HEMOGLOBIN QUEBEC-CHORI; HEMOGLOBIN CHORI; HEMOGLOBIN D (IBADAN)
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN QUEBEC-CHORI; HEMOGLOBIN CHORI; HEMOGLOBIN D (IBADAN)
}}{{PMID Auto
|PMID=457424
|Title=Hemoglobin D Ibadan trait in combination with sigma beta thalassemia.
}}

{{PMID Auto
|PMID=1891024
|Title=Sickle cell disease in a patient with sickle cell trait and compound heterozygosity for hemoglobin S and hemoglobin Quebec-Chori.
}}