{{Rsnum
|rsid=35348864
|Chromosome=11
|Orientation=minus
|geno1=(-;-)
|geno2=(-;CGG)
|geno3=(CGG;CGG)
|Gene=HBB
|position=5226798
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=35348864
|variant=0468
}}

{{ClinVar
|rsid=35348864
|Reversed=1
|FwdALT=GGC
|REF=G
|ALT=GCCG
|RSPOS=5248028
|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.5248028_5248029insCCG
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016821.24
|CLNDBN=Beta-thalassemia dominant
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=836; 141900.0468
|Disease=Beta-thalassemia dominant
}}

{{PMID Auto
|PMID=8703815
|Title=The dominant beta-thalassaemia in a Spanish family is due to a frameshift that introduces an extra CGG codon ( = arginine) at the 5' end of the second exon.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}