{{Rsnum
|rsid=33935445
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBB
|position=5226978
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33935445
|variant=0251
}}
{{omim
|id=141900
|rsnum=33935445
|variant=0264
}}{{ClinVar
|rsid=33935445
|Reversed=1
|FwdREF=T
|FwdALT=C,G
|REF=A
|ALT=C,G
|RSPOS=5248208
|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.5248208A>C; NC_000011.9:g.5248208A>G
|CLNORIGIN=1
|CLNSRCID=
243; 141900.0264; 244; 141900.0251
|CLNSIG=255
|CLNCUI=
|CLNACC=
RCV000016604.1; RCV000016584.1
|Tags=RV;PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNDBN=HEMOGLOBIN SOGN; HEMOGLOBIN SAKI
|CLNSRC=HBVAR; OMIM Allelic Variant
|Disease=HEMOGLOBIN SOGN; HEMOGLOBIN SAKI
}}{{PMID Auto
|PMID=2366586
|Title=Two families with hemoglobin Sogn, beta(A11)14 Leu----Arg, in Minnesota and Indiana: hematologic, functional, and biosynthetic features.
}}

{{PMID Auto
|PMID=4994348
|Title=Hb Sogn (beta 14 arginine). Haematological and genetical studies.
}}

{{PMID Auto
|PMID=5710451
|Title=Haemoglobin Sogn (beta 14 arginine) a new haemoglobin variant.
}}

{{PMID Auto
|PMID=8811316
|Title=Hb Sogn or alpha 2 beta 2 14(A11)Leu-->Arg in combination with an alpha-thalassemia heterozygosity.
}}

{{PMID Auto
|PMID=237566
|Title=Haemoglobin Saki alpha 2 beta 2 14 Leu-Pro(a11) structure and function.
}}

{{PMID Auto
|PMID=998617
|Title=Thalassemia intermedia caused by heterozygosity for both beta-thalassemia and hemoglobin Saki [beta 14 (A11) Leu replaced by Pro].
}}