Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10757274
rs10757274
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
G 0.900 GeneticVariation GWASDB Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease. 22751097

2012

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: rs1333049
rs1333049
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
C 0.900 GeneticVariation GWASDB Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. 24262325

2014

dbSNP: rs1333049
rs1333049
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.900 GeneticVariation GWASDB A genome-wide association study of a coronary artery disease risk variant. 23364394

2013

dbSNP: rs1333049
rs1333049
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.900 GeneticVariation GWASDB Large-scale association analysis identifies new risk loci for coronary artery disease. 23202125

2013

dbSNP: rs1333049
rs1333049
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.900 GeneticVariation GWASDB Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease. 22751097

2012

dbSNP: rs1333049
rs1333049
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.900 GeneticVariation GWASDB A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex. 22319020

2012

dbSNP: rs1333049
rs1333049
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
C 0.900 GeneticVariation GWASDB A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease. 21606135

2011

dbSNP: rs1333049
rs1333049
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.900 GeneticVariation GWASDB Large-scale gene-centric analysis identifies novel variants for coronary artery disease. 21966275

2011

dbSNP: rs1333049
rs1333049
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.900 GeneticVariation GWASDB Two-marker association tests yield new disease associations for coronary artery disease and hypertension. 21626137

2011

dbSNP: rs1333049
rs1333049
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.900 GeneticVariation GWASDB Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. 21347282

2011

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: rs4977756
rs4977756
CUI: C0017638
Disease: Glioma
Glioma
G 0.900 GeneticVariation GWASDB Genome-wide association study of glioma and meta-analysis. 22886559

2012

dbSNP: rs4977756
rs4977756
CUI: C0017638
Disease: Glioma
Glioma
0.900 GeneticVariation GWASDB Chromosome 7p11.2 (EGFR) variation influences glioma risk. 21531791

2011

dbSNP: rs4977756
rs4977756
CUI: C0017638
Disease: Glioma
Glioma
G 0.900 GeneticVariation GWASDB We identified five risk loci for glioma at 5p15.33 (rs2736100, TERT; P = 1.50 x 10(-17)), 8q24.21 (rs4295627, CCDC26; P = 2.34 x 10(-18)), 9p21.3 (rs4977756, CDKN2A-CDKN2B; P = 7.24 x 10(-15)), 20q13.33 (rs6010620, RTEL1; P = 2.52 x 10(-12)) and 11q23.3 (rs498872, PHLDB1; P = 1.07 x 10(-8)). 19578367

2009

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
G 0.880 GeneticVariation GWASDB Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. 19198609

2009

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: rs1333040
rs1333040
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm
T 0.840 GeneticVariation GWASDB Genome-wide association study of intracranial aneurysm identifies three new risk loci. 20364137

2010

dbSNP: rs1333040
rs1333040
CUI: C0007766
Disease: Intracranial Aneurysm
Intracranial Aneurysm
T 0.840 GeneticVariation GWASDB Susceptibility loci for intracranial aneurysm in European and Japanese populations. 18997786

2008

dbSNP: rs4977574
rs4977574
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.840 GeneticVariation GWASDB A genome-wide association study of a coronary artery disease risk variant. 23364394

2013

dbSNP: rs4977574
rs4977574
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.840 GeneticVariation GWASDB Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease. 22751097

2012

dbSNP: rs4977574
rs4977574
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.840 GeneticVariation GWASDB Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. 21347282

2011

dbSNP: rs4977574
rs4977574
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
G 0.840 GeneticVariation GWASDB A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. 21378988

2011