rs397514679, SYN1

N. diseases: 9
Disease: Dyslexia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Dyslexia
CUI: C0476254
Disease: Dyslexia
0.010 GeneticVariation BEFREE A new Q555X mutation on the SYN1 gene was recently found in several members of a family segregating dyslexia, epilepsy, and autism spectrum disorder. 29671924 2018