Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11066015
rs11066015
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C0010068
Disease:
Coronary heart disease
A 0.800 GeneticVariation GWASDB A genome-wide association study of a coronary artery disease risk variant. 23364394 2013
dbSNP: rs11066015
rs11066015
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C0010068
Disease:
Coronary heart disease
A 0.800 GeneticVariation GWASCAT A genome-wide association study of a coronary artery disease risk variant. 23364394 2013
dbSNP: rs61941274
rs61941274
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C0242383
Disease:
Age related macular degeneration
0.710 GeneticVariation BEFREE In addition, 1 genetic variant (rs61941274) was found to be associated with conversion to neovascular AMD. 31021381 2019
dbSNP: rs61941274
rs61941274
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C0242383
Disease:
Age related macular degeneration
0.710 GeneticVariation GWASCAT A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants. 26691988 2016
dbSNP: rs527760788
rs527760788
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C0200638
Disease:
Eosinophil count procedure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6490294
rs6490294
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C0032181
Disease:
Platelet Count measurement
0.700 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs11066015
rs11066015
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C0202239
Disease:
Uric acid measurement (procedure)
A 0.700 GeneticVariation GWASCAT Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. 29124443 2018
dbSNP: rs4766897
rs4766897
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C0337428
Disease:
Fibrinogen assay
0.700 GeneticVariation GWASCAT Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study. 28107422 2017
dbSNP: rs61941274
rs61941274
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C1536085
Disease:
Geographic Atrophy
0.700 GeneticVariation GWASCAT A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants. 26691988 2016
dbSNP: rs61941274
rs61941274
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C0271084
Disease:
Exudative age-related macular degeneration
0.700 GeneticVariation GWASCAT A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants. 26691988 2016
dbSNP: rs61941274
rs61941274
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C2237660
Disease:
exudative macular degeneration
0.700 GeneticVariation GWASCAT A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants. 26691988 2016
dbSNP: rs11066015
rs11066015
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C0001948
Disease:
Alcohol consumption
0.700 GeneticVariation GWASDB Genome-wide testing of putative functional exonic variants in relationship with breast and prostate cancer risk in a multiethnic population. 23555315 2013
dbSNP: rs608848
rs608848
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs609230
rs609230
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs617044
rs617044
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs630616
rs630616
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs634389
rs634389
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs640783
rs640783
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs642898
rs642898
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs6490294
rs6490294
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C0032181
Disease:
Platelet Count measurement
A 0.700 GeneticVariation GWASCAT A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans. 22423221 2012
dbSNP: rs6490294
rs6490294
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C0200665
Disease:
Platelet mean volume determination (procedure)
A 0.700 GeneticVariation GWASDB A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans. 22423221 2012
dbSNP: rs649406
rs649406
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs659964
rs659964
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs7962138
rs7962138
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs11066008
rs11066008
Entrez Id: 80724
Gene Symbol: ACAD10
ACAD10
CUI: C0546837
Disease:
Malignant neoplasm of esophagus
0.700 GeneticVariation GWASDB Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. 21642993 2011