Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6853
Gene Symbol: SYN1
SYN1 		0.700 Biomarker disease GENOMICS_ENGLAND SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function. 21441247 2011
Entrez Id: 6853
Gene Symbol: SYN1
SYN1 		0.700 GermlineCausalMutation disease ORPHANET Identification of a mutation in synapsin I, a synaptic vesicle protein, in a family with epilepsy. 14985377 2004
Entrez Id: 6853
Gene Symbol: SYN1
SYN1 		0.700 GeneticVariation disease CLINVAR
Entrez Id: 6853
Gene Symbol: SYN1
SYN1 		0.700 Biomarker disease CTD_human
Entrez Id: 6853
Gene Symbol: SYN1
SYN1 		0.700 CausalMutation disease CLINVAR
Entrez Id: 6853
Gene Symbol: SYN1
SYN1 		0.700 Biomarker disease GENOMICS_ENGLAND