TDP2, tyrosyl-DNA phosphodiesterase 2, 51567

N. diseases: 65; N. variants: 6
Disease: Dyslexia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0476254
Disease: Dyslexia
Dyslexia 		0.030 GeneticVariation disease BEFREE Interestingly, healthy subjects bearing the KIAA0319/TTRAP/THEM2 variants previously identified as enhancing the risk of dyslexia showed a reduced left-hemispheric asymmetry of the STS. 22262880 2012
CUI: C0476254
Disease: Dyslexia
Dyslexia 		0.030 Biomarker disease BEFREE Genes on chromosome 6p22, including DCDC2, KIAA0319, and TTRAP, have been identified as RD associated genes. 22750057 2012
CUI: C0476254
Disease: Dyslexia
Dyslexia 		0.030 GeneticVariation disease BEFREE We have recently identified a risk haplotype associated with dyslexia on chromosome 6p22.2 which spans the TTRAP gene and portions of THEM2 and KIAA0319. 16600991 2006