{{Rsnum
|rsid=79804069
|Gene=ALB
|Chromosome=4
|position=73412027
|Orientation=plus
|GMAF=0.0004591
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=ALB
}}{{omim
|id=103600
|rsnum=79804069
|variant=0043
}}{{ClinVar
|rsid=79804069
|Reversed=0
|FwdREF=A
|FwdALT=C
|REF=A
|ALT=C
|RSPOS=74277744
|CHROM=4
|GMAF=0.0005
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050268000000000016110100
|GENEINFO=ALB:213
|GENE_NAME=ALB
|GENE_ID=213
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.74277744A>C
|CLNORIGIN=0
|CLNSIG=255
|Tags=PM;PMC;S3D;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNACC=RCV000019888.1
|CLNDBN=ALBUMIN TRADATE 2
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=103600.0043
|COMMON=0
|Disease=ALBUMIN TRADATE 2
}}{{PMID|8022807|OA=1
}} Genetic variants of human serum albumin in Italy: point mutants and a carboxyl-terminal variant.