RAN, RAN, member RAS oncogene family, 5901

N. diseases: 87; N. variants: 2
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0476254
Disease: Dyslexia
Dyslexia
0.030 Biomarker disease BEFREE Results showed first that the dyslexia group was slower than the control group on all RAN tasks and the differences remained significant after controlling for discrete naming time. 29511958 2018
CUI: C0476254
Disease: Dyslexia
Dyslexia
0.030 GeneticVariation disease BEFREE The first three poor reader profiles were more characterized by variable environmental risk factor, while the fourth, PA-RAN poor reader subtype showed a significantly strong familial risk for dyslexia. 26922163 2017
CUI: C0476254
Disease: Dyslexia
Dyslexia
0.030 GeneticVariation disease BEFREE As part of a broad effort to identify genetic contributors to dyslexia, we performed combined oligogenic segregation and linkage analyses of measures of RAN and RAS in a family-based cohort ascertained through probands with dyslexia. 24807833 2014