SYN1, synapsin I, 6853

N. diseases: 80; N. variants: 16
Disease: Autistic Disorder ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397514680
rs397514680
Entrez Id: 6853
Gene Symbol: SYN1
SYN1
CUI: C0004352
Disease:
Autistic Disorder 		0.010 GeneticVariation BEFREE Additional mutations in SYN1 (A51G, A550T and T567A) were found in 1.0 and 3.5% of French-Canadian individuals with autism and epilepsy, respectively. 21441247 2011