{{Rsnum
|rsid=77892378
|Chromosome=4
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ALB
|position=73406760
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALB
}}{{omim
|id=103600
|rsnum=77892378
|variant=0056
}}{{ClinVar
|rsid=77892378
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=74272477
|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.74272477T>C
|CLNORIGIN=0
|CLNSIG=5
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000019900.26
|CLNDBN=Hyperthyroxinemia, dysalbuminemic
|CLNDSDB=MedGen
|CLNDSDBID=C1863119
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=103600.0056
|Disease=Hyperthyroxinemia
}}{{PMID Auto
|PMID=9589637
|Title=Familial dysalbuminemic hypertriiodothyroninemia: a new, dominantly inherited albumin defect.
}}