Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs16139
rs16139
NPY ; LOC107986777
0.050 GeneticVariation BEFREE Neuropeptide Y Leu7Pro polymorphism associated with the metabolic syndrome and its features in patients with coronary artery disease. 22308535

2013
dbSNP: rs16139
rs16139
NPY ; LOC107986777
0.050 GeneticVariation BEFREE High frequency of Neuropeptide Y Leu7Pro polymorphism in an Iranian population and its association with coronary artery disease. 22289186

2012
dbSNP: rs16139
rs16139
NPY ; LOC107986777
0.050 GeneticVariation BEFREE The Leu7Pro substitution has been linked to cardiovascular disease, but it is unknown whether the Pro7 allele is associated with increased or decreased risk of coronary heart disease (CHD). 18054939

2008
dbSNP: rs16139
rs16139
NPY ; LOC107986777
0.050 GeneticVariation BEFREE We conclude that the Leu7Pro polymorphism may contribute to the genetic susceptibility to diabetic nephropathy and CHD in type 1 diabetic patients, possibly by influencing glycemic control and triglycerides. 14747236

2004
dbSNP: rs16139
rs16139
NPY ; LOC107986777
0.050 GeneticVariation BEFREE Association of leucine 7 to proline 7 polymorphism in the preproneuropeptide Y with serum lipids in patients with coronary heart disease. 11914038

2002