MED1, mediator complex subunit 1, 5469

N. diseases: 88; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs146644295
rs146644295
Entrez Id: 5469
Gene Symbol: MED1
MED1
CUI: C0004096
Disease:
Asthma 		C 0.700 GeneticVariation GWASCAT Shared genetics of asthma and mental health disorders: a large-scale genome-wide cross-trait analysis. 31619474 2019
dbSNP: rs6503513
rs6503513
Entrez Id: 5469
Gene Symbol: MED1
MED1
CUI: C0596887
Disease:
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs7212715
rs7212715
Entrez Id: 5469
Gene Symbol: MED1
MED1
CUI: C0201976
Disease:
Creatinine measurement, serum (procedure) 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs7212715
rs7212715
Entrez Id: 5469
Gene Symbol: MED1
MED1
CUI: C0017654
Disease:
Glomerular Filtration Rate 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs6503513
rs6503513
Entrez Id: 5469
Gene Symbol: MED1
MED1
CUI: C0008312
Disease:
Primary biliary cirrhosis 		0.700 GeneticVariation GWASDB Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. 21399635 2011
dbSNP: rs9646419
rs9646419
Entrez Id: 5469
Gene Symbol: MED1
MED1
CUI: C0008312
Disease:
Primary biliary cirrhosis 		0.700 GeneticVariation GWASDB Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. 21399635 2011