rs17690703, MAPT-AS1

N. diseases: 4
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Idiopathic Pulmonary Fibrosis
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
0.800 GeneticVariation GWASDB Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study. 24429156 2013
Idiopathic Pulmonary Fibrosis
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
0.800 GeneticVariation GWASCAT Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study. 24429156 2013
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
0.700 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000 2012
Corpuscular Hemoglobin Concentration Mean
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.700 GeneticVariation GWASDB Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. 22438815 2012
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.700 GeneticVariation GWASDB Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. 21738487 2011
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
0.700 GeneticVariation GWASDB Genome-wide association study reveals genetic risk underlying Parkinson's disease. 19915575 2009