NTM, neurotrimin, 50863

N. diseases: 58; N. variants: 27
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0523953
Disease: Cardiac troponin T measurement
Cardiac troponin T measurement
0.100 GeneticVariation phenotype GWASDB Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies. 23247143 2013
CUI: C0523953
Disease: Cardiac troponin T measurement
Cardiac troponin T measurement
0.100 GeneticVariation phenotype GWASCAT Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies. 23247143 2013