{{Rsnum
|rsid=33933298
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBB
|position=5226597
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33933298
|variant=0151
}}{{ClinVar
|rsid=33933298
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=5247827
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000011.9:g.5247827C>T
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016443.1; RCV000016444.1; RCV000016445.1; RCV000016446.24; RCV000016807.1
|CLNDBN=HEMOGLOBIN KOLN; HEMOGLOBIN UBE-1; HEMOGLOBIN SAN FRANCISCO (PACIFIC); Heinz body hemolytic anemia; HEMOGLOBIN MEDICINE LAKE
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141900.0151; 141900.0452
|Disease=HEMOGLOBIN KOLN; HEMOGLOBIN UBE-1; HEMOGLOBIN SAN FRANCISCO (PACIFIC); Heinz body hemolytic anemia; HEMOGLOBIN MEDICINE LAKE
}}{{PMID Auto
|PMID=2283293
|Title=Unstable hemoglobins.
}}

{{PMID Auto
|PMID=5881530
|Title=[Hemoglobin Koln disease: familial hypochromic hemolytic anemia with hemoglobin anomaly].
}}

{{PMID Auto
|PMID=5960324
|Title=Haemoglobin Koln (beta-98 valine--methionine): an unstable protein causing inclusion-body anaemia.
}}

{{PMID Auto
|PMID=9136923
|Title=Thromboembolic complication of splenectomy in unstable hemoglobin disorders: Hb Olmsted, Hb Koln.
}}