{{Rsnum
|rsid=41443947
|Chromosome=11
|Orientation=minus
|geno1=(CT;CT)
|geno2=(CT;G)
|geno3=(G;G)
|Gene=HBB
|position=5225698
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=41443947
|variant=0335
}}

{{ClinVar
|rsid=41443947
|Reversed=1
|FwdREF=CT
|FwdALT=G
|REF=CAG
|ALT=CC
|RSPOS=5246927
|CHROM=11
|dbSNPBuildID=127
|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.5246928_5246929delAGinsC
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016681.24; RCV000016682.1
|CLNDBN=beta0^ Thalassemia; HEMOGLOBIN GENEVA
|CLNDSDB=MedGen:SNOMED_CT
|CLNDSDBID=C0271980:86715000
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=949; 141900.0335
|Disease=beta0^ Thalassemia; HEMOGLOBIN GENEVA
}}

{{PMID Auto
|PMID=3401599
|Title=Inclusion body beta-thalassemia trait in a Swiss family is caused by an abnormal hemoglobin (Geneva) with an altered and extended beta chain carboxy-terminus due to a modification in codon beta 114.
}}

{{on chip | 23andMe v3}}