SCAP, SREBF chaperone, 22937

N. diseases: 35; N. variants: 3
Disease: Myocardial Infarction ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 GeneticVariation disease LHGDN SREBP-2 and SCAP isoforms and risk of early onset myocardial infarction. 17383658 2008
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 GeneticVariation disease BEFREE SREBP-2 and SCAP isoforms and risk of early onset myocardial infarction. 17383658 2008