{{Rsnum
|rsid=35894115
|Chromosome=11
|Orientation=minus
|geno1=(-;-)
|geno2=(-;A)
|geno3=(A;A)
|Gene=HBB
|position=5226748
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=35894115
|variant=0395
}}{{ClinVar
|rsid=35894115
|Reversed=1
|FwdALT=A
|REF=A
|ALT=AT
|RSPOS=5247978
|CHROM=11
|dbSNPBuildID=126
|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.5247978_5247979insT
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=141900.0395
|CLNSIG=5
|CLNCUI=C0005283
|CLNDBN=beta Thalassemia
|Disease=beta Thalassemia
|CLNACC=RCV000016744.24
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1426:C0005283:613985:848:65959000
}}{{PMID Auto
|PMID=1698102
|Title=Observations on the levels of Hb A2 in patients with different beta-thalassemia mutations and a delta chain variant.
}}

{{PMID Auto
|PMID=2283303
|Title=A novel frameshift mutation [FSC 47 (+A)] causing beta-thalassemia in a Surinam patient.
}}