HPN, hepsin, 3249

N. diseases: 57; N. variants: 9
Disease: Serum albumin measurement ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.100 GeneticVariation phenotype GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.100 GeneticVariation phenotype GWASDB Discovery and fine mapping of serum protein loci through transethnic meta-analysis. 23022100 2012
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.100 GeneticVariation phenotype GWASCAT Discovery and fine mapping of serum protein loci through transethnic meta-analysis. 23022100 2012