DisGeNET - a database of gene-disease associations

Epilepsy, C0014544

Variant: rs3773364 ×

Source: ALL

Results per page

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

Variant

Gene

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs3773364

SYN2

0.030

GeneticVariation

BEFREE

No significant association was found between rs2920502 and rs3773364-rs3755724-rs2920502 haplotypes for susceptibility to epilepsy in each ethnicity.

25595263

2015

dbSNP:

rs3773364

SYN2

0.030

GeneticVariation

BEFREE

Our study indicated that SYN2 rs3773364 A>G polymorphism is not a risk factor for susceptibility to epilepsy.

21465568

2011

dbSNP:

rs3773364

SYN2

0.030

GeneticVariation

BEFREE

We selected rs3773364 A>G polymorphism in SYN2 gene and analyzed its distribution in north Indian patients with epilepsy and control subjects.

20034013

2010