Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2266788
rs2266788
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
C 0.800 GeneticVariation GWASDB A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. 21386085

2011

dbSNP: rs2266788
rs2266788
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
A 0.800 GeneticVariation GWASDB A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. 21386085

2011

dbSNP: rs2266788
rs2266788
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
C 0.800 GeneticVariation GWASDB A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. 21386085

2011

dbSNP: rs2075290
rs2075290
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
C 0.800 GeneticVariation GWASDB A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. 21386085

2011

dbSNP: rs2075290
rs2075290
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
C 0.800 GeneticVariation GWASDB A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. 21386085

2011

dbSNP: rs12286037
rs12286037
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
C 0.800 GeneticVariation GWASDB A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. 21386085

2011

dbSNP: rs11823543
rs11823543
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
A 0.800 GeneticVariation GWASDB A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. 21386085

2011

dbSNP: rs964184
rs964184
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
G 0.800 GeneticVariation GWASDB A genome wide association study identifies common variants associated with lipid levels in the Chinese population. 24386095

2013

dbSNP: rs964184
rs964184
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 GeneticVariation GWASDB A genome-wide association and gene-environment interaction study for serum triglycerides levels in a healthy Chinese male population. 22171074

2012

dbSNP: rs964184
rs964184
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
G 0.810 GeneticVariation GWASDB A previously known lipid locus, APOA1/C3/A4/A5 gene cluster region (SNP rs964184), was associated with MetS in all 4 study samples (P=7.23×10(-9) in meta-analysis). 22399527

2012

dbSNP: rs964184
rs964184
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
G 0.800 GeneticVariation GWASDB Amerindian-specific regions under positive selection harbour new lipid variants in Latinos. 24886709

2014

dbSNP: rs964184
rs964184
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides 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 Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010

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

2010

dbSNP: rs964184
rs964184
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
G 0.800 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010

dbSNP: rs964184
rs964184
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
G 0.700 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010

dbSNP: rs964184
rs964184
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
G 0.700 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 Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906

2009

dbSNP: rs964184
rs964184
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
G 0.800 GeneticVariation GWASDB Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906

2009

dbSNP: rs964184
rs964184
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
G 0.700 GeneticVariation GWASDB Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906

2009

dbSNP: rs964184
rs964184
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
C 0.800 GeneticVariation GWASDB Discovery and refinement of loci associated with lipid levels. 24097068

2013

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

2013

dbSNP: rs964184
rs964184
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
C 0.800 GeneticVariation GWASDB Discovery and refinement of loci associated with lipid levels. 24097068

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: rs2160669
rs2160669
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.800 GeneticVariation GWASDB Discovery and refinement of loci associated with lipid levels. 24097068

2013