{{Rsnum
|rsid=33972047
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBB
|position=5226963
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBB
}}{{omim
|id=141900
|rsnum=33972047
|variant=0168
}}

{{ClinVar
|rsid=33972047
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=5248193
|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.5248193T>C
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1426; 141900.0168
|CLNSIG=255
|CLNCUI=C0039730
|CLNDBN=HEMOGLOBIN MALAY; Beta-plus-thalassemia; Beta-malay-thalassemia; alpha Thalassemia
|Disease=HEMOGLOBIN MALAY; Beta-plus-thalassemia; Beta-malay-thalassemia; alpha Thalassemia
|CLNACC=RCV000016479.1; RCV000016480.24; RCV000016481.24; RCV000020338.1
|Tags=RV;PM;PMC;S3D;SLO;HD;GNO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1426:NBK1435:C0002312:604131:846:68913001
}}

{{PMID Auto
|PMID=2736244
|Title=Molecular characterization of beta-globin gene mutations in Malay patients with Hb E-beta-thalassaemia and thalassaemia major.
}}

{{PMID Auto
|PMID=2393018
|Title=The molecular basis of beta-thalassemia in Thailand: application to prenatal diagnosis.
|OA=1
}}

{{PMID Auto
|PMID=10861818
|Title=beta-thalassemia intermedia caused by compound heterozygosity for Hb Malay (beta codon 19 AAC-->AGC; asn-->Ser) and codons 41/42 (-CTTT) beta(0)-thalassemia mutation.
}}

{{on chip | HumanOmni1Quad}}