Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs886039269
rs886039269
DEPDC5
T 0.700 CausalMutation CLINVAR Mutations in the mammalian target of rapamycin pathway regulators NPRL2 and NPRL3 cause focal epilepsy. 26505888

2016
dbSNP: rs886039269
rs886039269
DEPDC5
T 0.700 CausalMutation CLINVAR Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy. 26704558

2016