Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7328626
rs7328626 		0.700 GeneticVariation GWASCAT GWAS identifies two susceptibility loci for lamotrigine-induced skin rash in patients with epilepsy. 26220383

2015
dbSNP: rs74308953
rs74308953
LOC102724929
A 0.700 GeneticVariation GWASCAT GWAS identifies two susceptibility loci for lamotrigine-induced skin rash in patients with epilepsy. 26220383

2015
dbSNP: rs7461897
rs7461897 		0.700 GeneticVariation GWASCAT GWAS identifies two susceptibility loci for lamotrigine-induced skin rash in patients with epilepsy. 26220383

2015
dbSNP: rs74912790
rs74912790 		A 0.700 GeneticVariation GWASCAT GWAS identifies two susceptibility loci for lamotrigine-induced skin rash in patients with epilepsy. 26220383

2015
dbSNP: rs7495694
rs7495694
LOC107984801
G 0.700 GeneticVariation GWASCAT GWAS identifies two susceptibility loci for lamotrigine-induced skin rash in patients with epilepsy. 26220383

2015
dbSNP: rs75078187
rs75078187
LOC100506422
0.700 GeneticVariation GWASCAT GWAS identifies two susceptibility loci for lamotrigine-induced skin rash in patients with epilepsy. 26220383

2015
dbSNP: rs79007183
rs79007183
CRAMP1
A 0.700 GeneticVariation GWASCAT GWAS identifies two susceptibility loci for lamotrigine-induced skin rash in patients with epilepsy. 26220383

2015
dbSNP: rs796051881
rs796051881
PEX5
CA 0.700 CausalMutation CLINVAR A novel type of rhizomelic chondrodysplasia punctata, RCDP5, is caused by loss of the PEX5 long isoform. 26220973

2015
dbSNP: rs9596837
rs9596837 		0.700 GeneticVariation GWASCAT GWAS identifies two susceptibility loci for lamotrigine-induced skin rash in patients with epilepsy. 26220383

2015
dbSNP: rs9596863
rs9596863
LINC00558
G 0.700 GeneticVariation GWASCAT GWAS identifies two susceptibility loci for lamotrigine-induced skin rash in patients with epilepsy. 26220383

2015
dbSNP: rs970510
rs970510
LOC102725148
0.700 GeneticVariation GWASCAT GWAS identifies two susceptibility loci for lamotrigine-induced skin rash in patients with epilepsy. 26220383

2015
dbSNP: rs111577701
rs111577701 		C 0.700 GeneticVariation GWASCAT Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies. 25087078

2014
dbSNP: rs28498976
rs28498976 		A 0.700 GeneticVariation GWASCAT Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies. 25087078

2014
dbSNP: rs492146
rs492146 		A 0.700 GeneticVariation GWASCAT A genome-wide association study and biological pathway analysis of epilepsy prognosis in a prospective cohort of newly treated epilepsy. 23962720

2014
dbSNP: rs535066
rs535066 		G 0.700 GeneticVariation GWASCAT Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies. 25087078

2014
dbSNP: rs61670327
rs61670327 		A 0.700 GeneticVariation GWASCAT A genome-wide association study and biological pathway analysis of epilepsy prognosis in a prospective cohort of newly treated epilepsy. 23962720

2014
dbSNP: rs6732655
rs6732655
SCN1A ; SCN1A-AS1
T 0.700 GeneticVariation GWASCAT Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies. 25087078

2014
dbSNP: rs72700966
rs72700966
PTPRD
C 0.700 GeneticVariation GWASCAT A genome-wide association study and biological pathway analysis of epilepsy prognosis in a prospective cohort of newly treated epilepsy. 23962720

2014
dbSNP: rs796053124
rs796053124
SCN2A
T 0.700 CausalMutation CLINVAR SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain. 20956790

2010
dbSNP: rs1057518988
rs1057518988
GRIN2B
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1064797102
rs1064797102
OTUD6B ; OTUD6B-AS1
G 0.700 CausalMutation CLINVAR

dbSNP: rs1064797103
rs1064797103
OTUD6B
G 0.700 GeneticVariation CLINVAR

dbSNP: rs121908869
rs121908869
TSHR ; CEP128
C 0.700 CausalMutation CLINVAR

dbSNP: rs121913578
rs121913578
MTR
T 0.700 GeneticVariation CLINVAR

dbSNP: rs139145929
rs139145929
CPA6 ; LOC102724708
A 0.700 GeneticVariation CLINVAR