Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1333049
rs1333049
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
C 0.900 GeneticVariation GWASDB Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. 17554300

2007

dbSNP: rs1333049
rs1333049
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
C 0.900 GeneticVariation GWASDB Of thousands of chromosomal loci studied, the same locus had the strongest association with coronary artery disease in both the WTCCC and the German studies: chromosome 9p21.3 (SNP, rs1333049) (P=1.80x10(-14) and P=3.40x10(-6), respectively). 17634449

2007

dbSNP: rs10757278
rs10757278
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
G 0.900 GeneticVariation GWASDB A common variant on chromosome 9p21 affects the risk of myocardial infarction. 17478679

2007

dbSNP: rs4977574
rs4977574
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.890 GeneticVariation GWASDB Genomewide association analysis of coronary artery disease. 17634449

2007

dbSNP: rs4977574
rs4977574
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.880 GeneticVariation GWASDB A common variant on chromosome 9p21 affects the risk of myocardial infarction. 17478679

2007

dbSNP: rs2891168
rs2891168
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.820 GeneticVariation GWASDB Genomewide association analysis of coronary artery disease. 17634449

2007

dbSNP: rs564398
rs564398
Diabetes Mellitus, Non-Insulin-Dependent
T 0.810 GeneticVariation GWASDB Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. 17463249

2007

dbSNP: rs1333042
rs1333042
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.810 GeneticVariation GWASDB Genomewide association analysis of coronary artery disease. 17634449

2007

dbSNP: rs10738607
rs10738607
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.810 GeneticVariation GWASDB A common variant on chromosome 9p21 affects the risk of myocardial infarction. 17478679

2007

dbSNP: rs2383207
rs2383207
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.770 GeneticVariation GWASDB A common variant on chromosome 9p21 affects the risk of myocardial infarction. 17478679

2007

dbSNP: rs1333045
rs1333045
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.730 GeneticVariation GWASDB A common variant on chromosome 9p21 affects the risk of myocardial infarction. 17478679

2007

dbSNP: rs1333040
rs1333040
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.720 GeneticVariation GWASDB A common variant on chromosome 9p21 affects the risk of myocardial infarction. 17478679

2007

dbSNP: rs9632884
rs9632884
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.710 GeneticVariation GWASDB Genomewide association analysis of coronary artery disease. 17634449

2007

dbSNP: rs564398
rs564398
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.710 GeneticVariation GWASDB Genomewide association analysis of coronary artery disease. 17634449

2007

dbSNP: rs518394
rs518394
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.710 GeneticVariation GWASDB Genomewide association analysis of coronary artery disease. 17634449

2007

dbSNP: rs7865618
rs7865618
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 GeneticVariation GWASDB Genomewide association analysis of coronary artery disease. 17634449

2007

dbSNP: rs7049105
rs7049105
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 GeneticVariation GWASDB Genomewide association analysis of coronary artery disease. 17634449

2007

dbSNP: rs7044859
rs7044859
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 GeneticVariation GWASDB Genomewide association analysis of coronary artery disease. 17634449

2007

dbSNP: rs6475608
rs6475608
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 GeneticVariation GWASDB A common variant on chromosome 9p21 affects the risk of myocardial infarction. 17478679

2007

dbSNP: rs6475606
rs6475606
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 GeneticVariation GWASDB Genomewide association analysis of coronary artery disease. 17634449

2007

dbSNP: rs643319
rs643319
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 GeneticVariation GWASDB Genomewide association analysis of coronary artery disease. 17634449

2007

dbSNP: rs523096
rs523096
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 GeneticVariation GWASDB Genomewide association analysis of coronary artery disease. 17634449

2007

dbSNP: rs496892
rs496892
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 GeneticVariation GWASDB Genomewide association analysis of coronary artery disease. 17634449

2007

dbSNP: rs1333048
rs1333048
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 GeneticVariation GWASDB Genomewide association analysis of coronary artery disease. 17634449

2007

dbSNP: rs1333048
rs1333048
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.700 GeneticVariation GWASDB A common variant on chromosome 9p21 affects the risk of myocardial infarction. 17478679

2007