{{Rsnum
|rsid=63750223
|Chromosome=11
|Orientation=minus
|geno1=(-;-)
|geno2=(-;GGTCTATTTTCCCACCCTTAGGCTG)
|geno3=(GGTCTATTTTCCCACCCTTAGGCTG;GGTCTATTTTCCCACCCTTAGGCTG)
|Gene=HBB
|position=5226796
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=63750223
|variant=0352
}}

{{ClinVar
|rsid=63750223
|Reversed=1
|FwdREF=GGTCTATTTTCCCACCCTTAGGCTG
|FwdALT=GGTCTATTTTCCCACCCTTAGGCTGC,C
|REF=GCAGCCTAAGGGTGGGAAAATAGACC
|ALT=G
|RSPOS=5248025
|CHROM=11
|dbSNPBuildID=137
|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.5248026_5248050del25
|CLNSIG=5
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016700.24; RCV000030009.1
|CLNDBN=beta0^ Thalassemia; beta Thalassemia
|CLNDSDB=MedGen:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0271980:86715000; NBK1426:C0005283:613985:848:65959000
|CLNORIGIN=1
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=974; 141900.0352
|Disease=beta0^ Thalassemia; beta Thalassemia
}}

{{PMID Auto
|PMID=6190800
|Title=Inactivation of an acceptor RNA splice site by a short deletion in beta-thalassemia.
}}

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