{{Rsnum
|rsid=63750067
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBA2
|position=173692
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA2
}}{{omim
|id=141850
|rsnum=63750067
|variant=0024
}}{{ClinVar
|rsid=63750067
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=223691
|CHROM=16
|dbSNPBuildID=137
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=HBA2:3040
|GENE_NAME=HBA2
|GENE_ID=3040
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.223691A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=141850.0024
|CLNSIG=255
|CLNCUI=CN077787
|CLNDBN=Alpha-thalassemia-2, nondeletional; Hemoglobin H disease, nondeletional
|Disease=Alpha-thalassemia-2; Hemoglobin H disease
|CLNACC=RCV000016933.25; RCV000022604.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=CN077787
}}{{PMID Auto
|PMID=1281602
|Title=Hb H disease caused by a homozygosity for the AATAAA-->AATAAG mutation in the polyadenylation site of the alpha 2-globin gene: hematological observations.
}}

{{PMID Auto
|PMID=1581238
|Title=Hb H disease in a Turkish family resulting from the interaction of a deletional alpha-thalassaemia-1 and a newly discovered poly A mutation.
}}

{{PMID Auto
|PMID=7701914
|Title=Molecular characterization of alpha-thalassemia determinants, beta-thalassemia alleles, and beta S haplotypes among Kuwaiti Arabs.
}}