{{Rsnum
|rsid=75002628
|Gene=ALB
|Chromosome=4
|position=73412007
|Orientation=plus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ALB
}}{{omim
|id=103600
|rsnum=75002628
|variant=0041
}}
{{omim
|id=103600
|rsnum=75002628
|variant=0055
}}{{ClinVar
|rsid=75002628
|Reversed=0
|FwdREF=G
|FwdALT=A,C
|REF=G
|ALT=A,C
|RSPOS=74277724
|CHROM=4
|GMAF=0.0009
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050268000000000016110100
|GENEINFO=ALB:213
|GENE_NAME=ALB
|GENE_ID=213
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000004.11:g.74277724G>A; NC_000004.11:g.74277724G>C
|CLNORIGIN=0
|CLNSRCID=
103600.0041; 103600.0055
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000019886.25; RCV000019899.25
|Tags=PM;PMC;S3D;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183; .
|CLNDBN=Hyperthyroxinemia, dysalbuminemic
|CLNDSDB=MedGen
|CLNDSDBID=C1863119
|CLNSRC=OMIM Allelic Variant
|COMMON=0
|Disease=Hyperthyroxinemia
}}{{PMID Auto
|PMID=8048949
|Title=An identical missense mutation in the albumin gene results in familial dysalbuminemic hyperthyroxinemia in 8 unrelated families.
}}

{{PMID Auto
|PMID=8064810
|Title=A point mutation in the human serum albumin gene results in familial dysalbuminaemic hyperthyroxinaemia.
|OA=1
}}

{{PMID Auto
|PMID=10728776
|Title=Familial dysalbuminemic byperthyroxinemia may result in altered warfarin pharmacokinetics.
}}

{{PMID Auto
|PMID=9329347
|Title=A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred.
}}