{{Rsnum
|rsid=35854892
|Chromosome=11
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=HBB
|position=5225617
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=35854892
|variant=0208
}}

{{ClinVar
|rsid=35854892
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=5246847
|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
|CLNHGVS=NC_000011.9:g.5246847A>C
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNACC=RCV000016531.1
|CLNDBN=HEMOGLOBIN OLMSTED
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141900.0208
|Disease=HEMOGLOBIN OLMSTED
}}

{{PMID Auto
|PMID=1125274
|Title=The amino acid substitution in Hb Olmsted: beta141 (H19) leucine yields arginine.
}}

{{PMID Auto
|PMID=5780360
|Title=Three families with unstable hemoglobinopathies (Koln, Olmsted and Santa Ana) causing hemolytic anemia with inclusion bodies and pigmenturia.
}}

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

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}