{{Rsnum
|rsid=41514946
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HBA2
|position=173573
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HBA2
}}{{omim
|id=141850
|rsnum=41514946
|variant=0062
}}{{ClinVar
|rsid=41514946
|Reversed=0
|FwdREF=C
|FwdALT=A,G
|REF=C
|ALT=A,G
|RSPOS=223572
|CHROM=16
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050360000000000102110100
|GENEINFO=HBA2:3040
|GENE_NAME=HBA2
|GENE_ID=3040
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.223572C>A
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;S3D;SLO;GNO;OTHERKG;LSD;OM
|CLNACC=RCV000016974.1
|CLNDBN=Hemoglobin Val de Marne
|CLNDSDB=MedGen
|CLNDSDBID=C0251144
|CLNSRC=HBVAR; OMIM Allelic Variant
|CLNSRCID=201; 141800.0177; 141850.0062
|Disease=Hemoglobin Val de Marne
}}