{{Rsnum
|rsid=77050410
|Chromosome=4
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ALB
|position=73406741
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALB
}}{{omim
|id=103600
|rsnum=77050410
|variant=0033
}}{{ClinVar
|rsid=77050410
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=74272458
|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.74272458G>A
|CLNORIGIN=0
|CLNSIG=255
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000019878.1
|CLNDBN=ALBUMIN TORINO
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=103600.0033
|Disease=ALBUMIN TORINO
}}{{PMID|2247440|OA=1
}} Mutations in genetic variants of human serum albumin found in Italy.