Gene entry
ALB
albumin
- Chromosome
- 4
- Cytoband
- 4q13.3
- Variants (rsID)
- 16
ALB is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 4 (region 4q13.3). Its official name is “albumin”. The reference table lists 16 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs142714816Likely benignsingle nucleotide variantHyperthyroxinemia, familial dysalbuminemic
- rs72552709Othersingle nucleotide variantPROALBUMIN LILLE
- rs77645174Othersingle nucleotide variantALBUMIN CASTEL DI SANGRO
- rs78284052Uncertain significancesingle nucleotide variantAlloalbuminemia|Analbuminemia
- rs78538497Uncertain significancesingle nucleotide variantALBUMIN IOWA CITY 1|Hyperthyroxinemia, familial dysalbuminemic
- rs80008208Uncertain significancesingle nucleotide variantPROALBUMIN MALMO|Hyperthyroxinemia, familial dysalbuminemic
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.