{{Rsnum
|rsid=193922563
|Chromosome=11
|Orientation=minus
|geno1=(-;-)
|geno2=(-;TGGTCTATTTTCCCACCCTTAGGCT)
|geno3=(TGGTCTATTTTCCCACCCTTAGGCT;TGGTCTATTTTCCCACCCTTAGGCT)
|Gene=HBB
|position=5226797
|Gene_s=HBB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922563
|Reversed=1
|FwdREF=TGGTCTATTTTCCCACCCTTAGGCT
|FwdALT=
|REF=CAGCCTAAGGGTGGGAAAATAGACCA
|ALT=C
|RSPOS=5248026
|CHROM=11
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050060000000000002100200
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5248027_5248051del25
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=beta0^ Thalassemia; beta Thalassemia
|Disease=beta0^ Thalassemia; beta Thalassemia
|Tags=RV;PM;OTHERKG;LSD
|CLNACC=RCV000016700.24; RCV000030009.1
|CLNDSDB=MedGen:SNOMED_CT; GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0271980:86715000; NBK1426:C0005283:613985:848:65959000
|CLNSRCID=974; 141900.0352
|GENEINFO=HBB:3043
|GENE_ID=3043
|GENE_NAME=HBB
}}