{{Rsnum
|rsid=41529844
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=HBA2
|position=173562
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA2
}}{{omim
|id=141850
|rsnum=41529844
|variant=0017
}}{{ClinVar
|rsid=41529844
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=223561
|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.223561G>C
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000016926.1
|CLNDBN=HEMOGLOBIN SUN PRAIRIE
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=141850.0017
|Disease=HEMOGLOBIN SUN PRAIRIE
}}{{PMID Auto
|PMID=2079430
|Title=Hb Sun Prairie or alpha(2)130(H13)Ala----Pro beta 2, a new unstable variant occurring in low quantities.
}}

{{PMID Auto
|PMID=2079431
|Title=Hb Sun Prairie or alpha(2)130(H13)Ala----Pro beta 2; second observation in an Indian adult.
}}

{{PMID Auto
|PMID=8811313
|Title=Hb Sun Prairie: diagnostic pitfalls in thalassemic hemoglobinopathies.
}}