{{Rsnum
|rsid=35256489
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBB
|position=5225710
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=35256489
|variant=0262
}}

{{ClinVar
|rsid=35256489
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=5246940
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050368000000000502110100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5246940A>G
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;SLO;HD;GNO;OTHERKG;LSD;OM
|CLNACC=RCV000016598.1; RCV000016599.24; RCV000016600.24; RCV000029991.1
|CLNDBN=HEMOGLOBIN SHOWA-YAKUSHIJI; Beta-plus-thalassemia; Beta-showa-yakushiji thalassemia; Beta thalassemia major
|CLNDSDB=MedGen
|CLNDSDBID=C0599528
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=485; 141900.0262
|Disease=HEMOGLOBIN SHOWA-YAKUSHIJI; Beta-plus-thalassemia; Beta-showa-yakushiji thalassemia; Beta thalassemia major
}}

{{PMID Auto
|PMID=2822177
|Title=A novel globin structural mutant, Showa-Yakushiji (beta 110 Leu-Pro) causing a beta-thalassemia phenotype.
}}

{{PMID Auto
|PMID=3417300
|Title=A substitution of cytosine for thymine in codon 110 of the human beta-globin gene is a novel cause of beta-thalassemia phenotypes.
}}

{{PMID Auto
|PMID=9101288
|Title=beta-thalassemia mutations in Japanese and Koreans.
}}

{{PMID Auto
|PMID=12709369
|Title=Rapid detection of beta-globin gene mutations and polymorphisms by temporal temperature gradient gel electrophoresis.
}}

{{PMID Auto
|PMID=18294253
|Title=Analysis of beta globin mutations in the Indian population: presence of rare and novel mutations and region-wise heterogeneity.
}}

{{PMID Auto
|PMID=20437613
|Title=Mutations of a country: a mutation review of single gene disorders in the United Arab Emirates (UAE).
}}

{{PMID Auto
|PMID=2634667
|Title=Characterization of beta-thalassemia mutations among the Japanese.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}