{{Rsnum
|rsid=41457746
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HBA2
|position=173123
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA2
}}{{omim
|id=141850
|rsnum=41457746
|variant=0056
}}

{{ClinVar
|ALT=G
|CHROM=16
|CLNACC=RCV000016968.25
|CLNALLE=1
|CLNDBN=Alpha-thalassemia, dutch type
|CLNHGVS=NC_000016.9:g.223122A>G
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=1066; 141850.0056
|Disease=Alpha-thalassemia
|FwdALT=G
|FwdREF=A
|GENEINFO=HBA2:3040
|GENE_ID=3040
|GENE_NAME=HBA2
|REF=A
|RSPOS=223122
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000000002110100
|WGT=0
|dbSNPBuildID=127
|rsid=41457746
}}

{{PMID Auto
|PMID=8943885
|Title=An IVS1-116 (A-->G) acceptor splice site mutation in the alpha 2 globin gene causing alpha + thalassaemia in two Dutch families.
}}

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