{{Rsnum
|rsid=41466346
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBA2
|position=173270
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA2
}}{{omim
|id=141850
|rsnum=41466346
|variant=0035
}}

{{ClinVar
|rsid=41466346
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=223269
|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.223269C>G
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016946.1
|CLNDBN=HEMOGLOBIN CONAKRY
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141850.0035
|Disease=HEMOGLOBIN CONAKRY
}}

{{PMID Auto
|PMID=9886305
|Title=A new sickle cell disease phenotype associating Hb S trait, severe pyruvate kinase deficiency (PK Conakry), and an alpha2 globin gene variant (Hb Conakry).
}}

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