PPID, peptidylprolyl isomerase D, 5481

N. diseases: 72; N. variants: 2
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 GWASDB A genome-wide perspective of genetic variation in human metabolism. 20037589 2010