{{Rsnum
|rsid=35703285
|Chromosome=11
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=HBB
|position=5225740
|Gene_s=HBB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=35703285
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=5246970
|CHROM=11
|dbSNPBuildID=126
|SSR=0
|SAO=1
|VP=0x050168000000000002100100
|GENEINFO=HBB:3043
|GENE_NAME=HBB
|GENE_ID=3043
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.5246970A>C
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=beta Thalassemia
|Disease=beta Thalassemia
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD
|CLNACC=RCV000029980.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1426:C0005283:613985:848:65959000
}}

{{PMID Auto
|PMID=12709
|Title=["Enzymology" Commission: recommendations for the measurement of the catalytic activity of aspartate aminotransferase in serum at 30degreesC (Document b stage 3)].
}}

{{PMID Auto
|PMID=15933066
|Title=Patients with thalassemia in the United States.
|OA=1
}}

{{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=19205975
|Title=Hematological and molecular analysis of novel and rare beta-thalassemia mutations in the Indian population.
}}

{{PMID Auto
|PMID=20230396
|Title=Epidemiology of beta-thalassaemia in Western India: mapping the frequencies and mutations in sub-regions of Maharashtra and Gujarat.
}}

{{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=1772786
|Title=Rare beta-thalassaemia mutations in Asian indians.
}}

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