{{Rsnum
|rsid=33991472
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBB
|position=5226716
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33991472
|variant=0040
}}
{{omim
|id=141900
|rsnum=33991472
|variant=0308
}}

{{ClinVar
|rsid=33991472
|Reversed=1
|FwdREF=C
|FwdALT=A,G
|REF=G
|ALT=C,T
|RSPOS=5247946
|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.5247946G>C
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016651.1; RCV000016652.1; RCV000030905.1
|CLNDBN=HEMOGLOBIN YUKUHASHI; HEMOGLOBIN DHOFAR; HEMOGLOBIN ZIGUINCHOR
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141900.0040; 141900.0308
|Disease=HEMOGLOBIN YUKUHASHI; HEMOGLOBIN DHOFAR; HEMOGLOBIN ZIGUINCHOR
}}

{{PMID Auto
|PMID=5684629
|Title=Haemoglobin Dhofar--a new variant from Southern Arabia.
}}

{{PMID Auto
|PMID=7786794
|Title=Haemoglobin Dhofar is linked to the codon 29 C-->T (IVS-1 nt-3) splice mutation which causes beta+ thalassaemia.
}}

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