{{Rsnum
|rsid=34726542
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HBB
|position=5225679
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=34726542
|variant=0239
}}{{ClinVar
|rsid=34726542
|Reversed=1
|FwdREF=A
|FwdALT=C
|REF=T
|ALT=G
|RSPOS=5246909
|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.5246909T>G
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016568.1; RCV000016569.1
|CLNDBN=HEMOGLOBIN RIYADH; HEMOGLOBIN KARATSU
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141900.0239
|Disease=HEMOGLOBIN RIYADH; HEMOGLOBIN KARATSU
}}{{PMID Auto
|PMID=511584
|Title=Hemoglobin Riyadh-beta 0-thalassemia in an Indian family.
}}

{{PMID Auto
|PMID=893129
|Title=Hemoglobin Riyadh in a Mexican American family of Spanish ancestry.
}}

{{PMID Auto
|PMID=1052171
|Title=Hemoglobin Riyadh--alpha2beta2 (120(GH3)Lys replaced by Asn). A new variant found in association with alpha-thalassemia and iron deficiency.
}}