{{Rsnum
|rsid=41341344
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HBA2
|position=173001
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA2
}}{{omim
|id=141850
|rsnum=41341344
|variant=0026
}}

{{ClinVar
|rsid=41341344
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=223000
|CHROM=16
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=HBA2:3040
|GENE_NAME=HBA2
|GENE_ID=3040
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.223000T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=141850.0026
|CLNSIG=255
|CLNCUI=CN077787
|CLNDBN=HEMOGLOBIN AGRINIO; Hemoglobin H disease, nondeletional
|Disease=HEMOGLOBIN AGRINIO; Hemoglobin H disease
|CLNACC=RCV000016937.1; RCV000022605.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=CN077787
}}

{{PMID Auto
|PMID=8136277
|Title=A base substitution (T-->C) in codon 29 of the alpha 2-globin gene causes alpha thalassaemia.
}}

{{PMID Auto
|PMID=8537235
|Title=Hb A2-Agrinio [delta 43(CD2)Glu-->Gly(GAG-->GGG)]: a new delta chain variant detected in a Greek family.
}}

{{PMID Auto
|PMID=9629496
|Title=An alpha-thalassemic hemoglobinopathy: homozygosity for the HB Agrinio alpha 2-globin chain variant.
}}

{{PMID Auto
|PMID=11042028
|Title=Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.
}}

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