Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs964184
rs964184
High density lipoprotein measurement
G 0.800 GeneticVariation GWASDB Genome-wide characterization of shared and distinct genetic components that influence blood lipid levels in ethnically diverse human populations. 23726366

2013

dbSNP: rs964184
rs964184
High density lipoprotein measurement
C 0.800 GeneticVariation GWASDB Discovery and refinement of loci associated with lipid levels. 24097068

2013

dbSNP: rs964184
rs964184
High density lipoprotein measurement
0.800 GeneticVariation GWASDB Here we apply an EMR-based phenotyping approach, within the context of routine care, to replicate several known associations between HDL-C and previously characterized genetic variants: CETP (rs3764261, p = 1.22e-25), LIPC (rs11855284, p = 3.92e-14), LPL (rs12678919, p = 1.99e-7), and the APOA1/C3/A4/A5 locus (rs964184, p = 1.06e-5), all adjusted for age, gender, body mass index (BMI), and smoking status. 21589926

2011

dbSNP: rs964184
rs964184
High density lipoprotein measurement
G 0.800 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010

dbSNP: rs964184
rs964184
High density lipoprotein measurement
G 0.800 GeneticVariation GWASDB Genetic variants influencing circulating lipid levels and risk of coronary artery disease. 20864672

2010

dbSNP: rs964184
rs964184
High density lipoprotein measurement
G 0.800 GeneticVariation GWASDB Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906

2009