{{Rsnum
|rsid=63751201
|Chromosome=11
|Orientation=minus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=HBB
|position=5225714
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=63751201
|variant=0422
}}{{ClinVar
|rsid=63751201
|Reversed=1
|FwdREF=G
|FwdALT=
|REF=AC
|ALT=A
|RSPOS=5246943
|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.5246944delC
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016687.24
|CLNDBN=beta0^ Thalassemia
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0271980:86715000
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=947; 141900.0340
|Disease=beta0^ Thalassemia
}}{{PMID Auto
|PMID=1586746
|Title=Dominant thalassemia-like phenotypes associated with mutations in exon 3 of the beta-globin gene.
}}