{{Rsnum
|rsid=35871407
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBB
|position=5225707
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=35871407
|variant=0270
}}

{{ClinVar
|rsid=35871407
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=5246937
|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
|CLNHGVS=NC_000011.9:g.5246937A>G
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016607.1
|CLNDBN=HEMOGLOBIN STANMORE
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141900.0270
|Disease=HEMOGLOBIN STANMORE
}}

{{PMID Auto
|PMID=1917537
|Title=A new unstable and low oxygen affinity hemoglobin variant: Hb Stanmore [beta 111(G13)Val----Ala].
}}

{{PMID Auto
|PMID=12828994
|Title=First case of a single heterozygote of an abnormal hemoglobin, Hb Stanmore, [beta111(G13)Val-->Ala].
}}

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