PPID, peptidylprolyl isomerase D, 5481

N. diseases: 72; N. variants: 2
Disease: Serum albumin measurement ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs8396
rs8396
Entrez Id: 2110;5481
Gene Symbol: ETFDH;PPID
ETFDH;PPID
CUI: C0523465
Disease:
Serum albumin measurement 		T 0.700 GeneticVariation GWASDB A genome-wide perspective of genetic variation in human metabolism. 20037589 2010