{{Rsnum
|rsid=41321345
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HBA2
|position=173599
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA2
}}{{omim
|id=141850
|rsnum=41321345
|variant=0003
}}

{{ClinVar
|rsid=41321345
|Reversed=0
|FwdREF=A
|FwdALT=C
|REF=A
|ALT=C
|RSPOS=223598
|CHROM=16
|dbSNPBuildID=127
|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.223598A>C
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016894.1
|CLNDBN=HEMOGLOBIN KOYA DORA
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141850.0003
|Disease=HEMOGLOBIN KOYA DORA
}}

{{PMID Auto
|PMID=1155453
|Title=Hemoglobin Koya Dora: high frequency of a chain termination mutant.
|OA=1
}}

{{PMID Auto
|PMID=1802886
|Title=Hemoglobinopathies among the Gond tribal groups of central India; interaction of alpha- and beta-thalassemia with beta chain variants.
}}

{{PMID Auto
|PMID=8251382
|Title=An IVS-I-117 (G-->A) acceptor splice site mutation in the alpha 1-globin gene is a nondeletional alpha-thalassaemia-2 determinant in an Indian population.
}}

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