ERG, ETS transcription factor ERG, 2078

N. diseases: 298; N. variants: 31
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2836411
rs2836411
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C0162871
Disease:
Aortic Aneurysm, Abdominal 		0.720 GeneticVariation BEFREE Associations between rs9316871and rs2836411 and AAA risk were replicated in the meta-analysis of the two independent cohorts, providing further support for the importance of these loci in the aetiology of AAA. 31680049 2020
dbSNP: rs2836411
rs2836411
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C0162871
Disease:
Aortic Aneurysm, Abdominal 		0.720 GeneticVariation BEFREE ERG is involved in vascular development, angiogenesis, and inflammation in atherosclerosis, therefore mechanistically, rs2836411 could contribute to AAA by modulating ERG levels. 31691800 2020
dbSNP: rs2836411
rs2836411
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C0162871
Disease:
Aortic Aneurysm, Abdominal 		T 0.720 GeneticVariation GWASCAT Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci. 27899403 2017
dbSNP: rs2836425
rs2836425
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C0026769
Disease:
Multiple Sclerosis 		0.710 GeneticVariation BEFREE Our study highlighted that people who are carrying genotypes including GG (SHMT1 rs4925166) and TC (ERG rs2836425) have the highest susceptibility chance for MS, respectively. 30456721 2019
dbSNP: rs2836425
rs2836425
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C0026769
Disease:
Multiple Sclerosis 		T 0.710 GeneticVariation GWASCAT Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation. 27386562 2016
dbSNP: rs1015022
rs1015022
Entrez Id: 2078;105372802
Gene Symbol: ERG;LOC105372802
ERG;LOC105372802
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs117870289
rs117870289
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C0428883
Disease:
Diastolic blood pressure 		T 0.700 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
dbSNP: rs117870289
rs117870289
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2836422
rs2836422
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs35042034
rs35042034
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs56180262
rs56180262
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs80109907
rs80109907
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs9977881
rs9977881
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C0029410
Disease:
Osteoarthritis of hip 		C 0.700 GeneticVariation GWASCAT Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data. 30664745 2019
dbSNP: rs9977881
rs9977881
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C0409959
Disease:
Osteoarthritis, Knee 		C 0.700 GeneticVariation GWASCAT Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data. 30664745 2019
dbSNP: rs78762153
rs78762153
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C0200641
Disease:
Blood basophil count (lab test) 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs117870289
rs117870289
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C0428883
Disease:
Diastolic blood pressure 		C 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878 2017
dbSNP: rs117910189
rs117910189
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C1318312
Disease:
Serum iron measurement 		T 0.700 GeneticVariation GWASCAT Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation? 28334935 2017
dbSNP: rs2836422
rs2836422
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2836422
rs2836422
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C0524587
Disease:
Mean Corpuscular Volume (result) 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2836441
rs2836441
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C0032181
Disease:
Platelet Count measurement 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs58030288
rs58030288
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C0200641
Disease:
Blood basophil count (lab test) 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs58030288
rs58030288
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C0200638
Disease:
Eosinophil count procedure 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs9982370
rs9982370
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C0021704
Disease:
Intelligence 		0.700 GeneticVariation GWASCAT "Results of a ""GWAS plus:"" general cognitive ability is substantially heritable and massively polygenic." 25383866 2014
dbSNP: rs2836439
rs2836439
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C0004352
Disease:
Autistic Disorder 		0.700 GeneticVariation GWASDB Individual common variants exert weak effects on the risk for autism spectrum disorders. 22843504 2012
dbSNP: rs2836389
rs2836389
Entrez Id: 2078
Gene Symbol: ERG
ERG
CUI: C0019163
Disease:
Hepatitis B 		0.700 GeneticVariation GWASDB A genome-wide association study of chronic hepatitis B identified novel risk locus in a Japanese population. 21750111 2011