{{Rsnum
|rsid=33962676
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBB
|position=5226972
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33962676
|variant=0123
}}{{ClinVar
|rsid=33962676
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=5248202
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000102110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5248202C>T
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNACC=RCV000016400.2
|CLNDBN=HEMOGLOBIN J (BALTIMORE)
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=247; 141900.0123
|Disease=HEMOGLOBIN J (BALTIMORE)
}}{{PMID Auto
|PMID=8226093
|Title=Rare beta chain hemoglobin variants found in Swedish patients during HBA1c analysis.
}}

{{PMID Auto
|PMID=8745435
|Title=Hb J-Baltimore [beta 16(A13)Gly-->Asp] associated with beta(+)-thalassemia in a Spanish family.
}}