DisGeNET - a database of gene-disease associations

rs3773364, SYN2

N. diseases: 2

Disease: idiopathic epilepsy ×

Source: ALL

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Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

idiopathic epilepsy

CUI:	C0391957
Disease:	idiopathic epilepsy

0.010

GeneticVariation

BEFREE

Association of intronic polymorphism rs3773364 A>G in synapsin-2 gene with idiopathic epilepsy.

2010