CEP295NL, CEP295 N-terminal like, 100653515

N. diseases: 6; N. variants: 11
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases 		0.100 GeneticVariation group GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.100 GeneticVariation phenotype GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis 		0.100 GeneticVariation disease GWASCAT Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease. 25017104 2014
CUI: C0013312
Disease: Dupuytren Contracture
Dupuytren Contracture 		0.100 GeneticVariation disease GWASCAT Wnt signaling and Dupuytren's disease. 21732829 2011
CUI: C4082974
Disease: Dupuytren's Disease
Dupuytren's Disease 		0.100 GeneticVariation disease GWASDB Wnt signaling and Dupuytren's disease. 21732829 2011
CUI: C2700366
Disease: Adiponectin Measurement
Adiponectin Measurement 		0.100 GeneticVariation phenotype GWASDB Adiponectin concentrations: a genome-wide association study. 20887962 2010