LCAT, lecithin-cholesterol acyltransferase, 3931

N. diseases: 94; N. variants: 41
Disease: Hypoalphalipoproteinemias ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1160100323
rs1160100323
Entrez Id: 3931
Gene Symbol: LCAT
LCAT
CUI: C0473527
Disease:
Hypoalphalipoproteinemias 		0.010 GeneticVariation BEFREE After renal transplantation, proband's lipid profile, HDL subclass distribution, and plasma cholesterol esterification were almost at normal levels, suggesting a mild contribution of the LCAT P406L variant to his pretransplantation severe hypoalphalipoproteinemia and impairment of plasma cholesterol esterification. 22658148 2012