{{Rsnum
|rsid=80002911
|Chromosome=4
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ALB
|position=73413451
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALB
}}{{omim
|id=103600
|rsnum=80002911
|variant=0049
}}{{ClinVar
|rsid=80002911
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=74279168
|CHROM=4
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050268000000000002110100
|GENEINFO=ALB:213
|GENE_NAME=ALB
|GENE_ID=213
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.74279168A>G
|CLNORIGIN=0
|CLNSIG=255
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000019893.1
|CLNDBN=ALBUMIN MALMO 10
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=103600.0049
|Disease=ALBUMIN MALMO 10
}}{{PMID Auto
|PMID=1518850
|Title=Alloalbuminemia in Sweden: structural study and phenotypic distribution of nine albumin variants.
|OA=1
}}