{{Rsnum
|rsid=1800580
|Chromosome=4
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=ALB
|position=73419640
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALB
}}{{omim
|id=103600
|rsnum=1800580
|variant=0038
}}

{{ClinVar
|rsid=1800580
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=74285357
|CHROM=4
|dbSNPBuildID=89
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=ALB:213
|GENE_NAME=ALB
|GENE_ID=213
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.74285357G>C
|CLNORIGIN=0
|CLNSIG=255
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000019883.1
|CLNDBN=ALBUMIN RUGBY PARK
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=103600.0038
|Disease=ALBUMIN RUGBY PARK
}}

{{PMID|1390939}} Albumin Rugby Park: a truncated albumin variant caused by a G-->C splice-site mutation in intron 13.

{{PMID|9392528}} Effect of genetic variation on the fatty acid-binding properties of human serum albumin and proalbumin.

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}