Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.100 GeneticVariation GWASDB Genetic variants influencing circulating lipid levels and risk of coronary artery disease. 20864672

2010

Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.100 GeneticVariation GWASDB Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci. 23505323

2013

Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.100 GeneticVariation GWASDB Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans. 18193044

2008

Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.100 GeneticVariation GWASDB Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides. 18193046

2008

Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.100 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010

Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.100 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012

Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.100 GeneticVariation GWASDB Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. 19060911

2009

Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.100 GeneticVariation GWASDB Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906

2009

Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.100 GeneticVariation GWASDB Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits. 21909109

2011

Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.100 GeneticVariation GWASDB Discovery and refinement of loci associated with lipid levels. 24097068

2013

Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.100 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219

2012

Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C0523744
Disease: Lipids measurement
Lipids measurement
0.100 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219

2012

Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.100 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012

Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.100 GeneticVariation GWASDB Biological, clinical and population relevance of 95 loci for blood lipids. 20686565

2010

Entrez Id: 19
Gene Symbol: ABCA1
ABCA1
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.100 GeneticVariation GWASDB Discovery and refinement of loci associated with lipid levels. 24097068

2013

Entrez Id: 154664
Gene Symbol: ABCA13
ABCA13
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement
0.100 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178

2013

Entrez Id: 24
Gene Symbol: ABCA4
ABCA4
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip
0.410 GeneticVariation GWASDB SNPs near two genes not previously associated with cleft lip with and without cleft palate (MAFB, most significant SNP rs13041247, with odds ratio (OR) per minor allele = 0.704, 95% CI 0.635-0.778, P = 1.44 x 10(-11); and ABCA4, most significant SNP rs560426, with OR = 1.432, 95% CI 1.292-1.587, P = 5.01 x 10(-12)) and two previously identified regions (at chromosome 8q24 and IRF6) attained genome-wide significance. 20436469

2010

Entrez Id: 24
Gene Symbol: ABCA4
ABCA4
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip
0.410 GeneticVariation GWASDB Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci. 22863734

2012

Entrez Id: 24
Gene Symbol: ABCA4
ABCA4
Low density lipoprotein cholesterol measurement
0.100 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012

Entrez Id: 24
Gene Symbol: ABCA4
ABCA4
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.100 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012

Entrez Id: 24
Gene Symbol: ABCA4
ABCA4
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.100 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622

2012

Entrez Id: 10347
Gene Symbol: ABCA7
ABCA7
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.500 GeneticVariation GWASDB Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. 24162737

2013

Entrez Id: 10347
Gene Symbol: ABCA7
ABCA7
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.500 GeneticVariation GWASDB Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. 21460841

2011

Entrez Id: 10347
Gene Symbol: ABCA7
ABCA7
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.500 GeneticVariation GWASDB Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans. 23571587

2013

Entrez Id: 10347
Gene Symbol: ABCA7
ABCA7
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.500 GeneticVariation GWASDB Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. 21460840

2011