{{Rsnum
|rsid=35699671
|Chromosome=11
|Orientation=minus
|geno1=(-;-)
|geno2=(-;GTG)
|geno3=(GTG;GTG)
|Gene=HBB
|position=5226790
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=35699671
|variant=0443
}}{{ClinVar
|rsid=35699671
|Reversed=1
|FwdREF=TGG
|FwdALT=
|REF=CCAC
|ALT=C
|RSPOS=5248019
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050168000000000002110200
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5248020_5248022delCAC
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016797.1
|CLNDBN=HEMOGLOBIN KOREA
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141900.0443
|Disease=HEMOGLOBIN KOREA
}}{{PMID Auto
|PMID=1911355
|Title=A spontaneous deletion of beta 33/34 Val in exon 2 of the beta globin gene (Hb Korea) produces the phenotype of dominant beta thalassaemia.
}}

{{PMID Auto
|PMID=9101288
|Title=beta-thalassemia mutations in Japanese and Koreans.
}}