{{Rsnum
|rsid=33952850
|Chromosome=11
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=HBB
|position=5226746
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33952850
|variant=0205
}}
{{omim
|id=141900
|rsnum=33952850
|variant=0421
}}{{ClinVar
|rsid=33952850
|Reversed=1
|FwdREF=T
|FwdALT=C,G
|REF=A
|ALT=C,G
|RSPOS=5247976
|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; 2
|CLNHGVS=NC_000011.9:g.5247976A>C; NC_000011.9:g.5247976A>G
|CLNORIGIN=1
|CLNSRCID=
328; 141900.0205; 329; 141900.0421
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016528.1; RCV000016772.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDBN=HEMOGLOBIN OKALOOSA; HEMOGLOBIN BAB-SAADOUN
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN OKALOOSA; HEMOGLOBIN BAB-SAADOUN
}}{{PMID Auto
|PMID=4748512
|Title=Hemoglobin Okaloosa (beta 48 (CD7) leucine leads to arginine). An unstable variant with low oxygen affinity.
|OA=1
}}

{{PMID Auto
|PMID=1517103
|Title=Hb Bab-Saadoun or alpha 2 beta (2)48(CD7)Leu----Pro, a mildly unstable variant found in an Arabian boy from Tunisia.
}}