{{Rsnum
|rsid=35117167
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBB
|position=5225605
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=35117167
|variant=0232
}}

{{ClinVar
|rsid=35117167
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=5246835
|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.5246835T>C
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNACC=RCV000016562.1
|CLNDBN=HEMOGLOBIN RAINIER
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141900.0232
|Disease=HEMOGLOBIN RAINIER
}}

{{PMID Auto
|PMID=478981
|Title=Hb Rainier or alpha 2 beta 2 (145 (HC2) Tyr replaced by Cys) observed in members of a Canadian family of Greek origin.
}}

{{PMID Auto
|PMID=3793825
|Title=Isolation of human haemoglobin variants with altered Bohr effect. Application to haemoglobin Rainier.
}}

{{PMID Auto
|PMID=5019947
|Title=Oxygen equilibrium and circular dichroism of hemoglobin-Rainer ( 2 2 1 45Tyr leads to Cys).
}}

{{PMID Auto
|PMID=5796352
|Title=Erythrocytosis associated with hemoglobin Rainier: oxygen equilibria and marrow regulation.
|OA=1
}}

{{PMID Auto
|PMID=10335979
|Title=Hb Rainier [beta145(HC2)Tyr-->Cys] in Italy. Characterization of the amino acid substitution and the DNA mutation.
}}

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