{{Rsnum
|rsid=63751218
|Chromosome=11
|Orientation=minus
|geno1=(AGTGA;AGTGA)
|geno2=(AGTGA;T)
|geno3=(T;T)
|Gene=HBB
|position=5226671
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=63751218
|variant=0472
}}

{{ClinVar
|rsid=63751218
|Reversed=1
|FwdREF=AGTGA
|FwdALT=T
|REF=ATCACT
|ALT=AA
|RSPOS=5247900
|CHROM=11
|dbSNPBuildID=137
|SSR=0
|SAO=1
|VP=0x050368000000000002110200
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5247901_5247905delTCACTinsA
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016826.24
|CLNDBN=beta0^ Thalassemia
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0271980:86715000
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=871; 141900.0472
|Disease=beta0^ Thalassemia
}}

{{PMID Auto
|PMID=9255617
|Title=Novel beta 0-thalassemia mutation in a Canadian woman of British descent (codons 72/73, -AGTGA, +T).
}}

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