Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894063
rs104894063
CHRNA2
0.800 GeneticVariation UNIPROT Increased sensitivity of the neuronal nicotinic receptor alpha 2 subunit causes familial epilepsy with nocturnal wandering and ictal fear. 16826524

2006
dbSNP: rs104894063
rs104894063
CHRNA2
T 0.800 CausalMutation CLINVAR

dbSNP: rs1018084204
rs1018084204
CHRNA2
0.700 GeneticVariation UNIPROT Mutation of CHRNA2 in a family with benign familial infantile seizures: Potential role of nicotinic acetylcholine receptor in various phenotypes of epilepsy. 25847220

2015
dbSNP: rs12721510
rs12721510
CRH
T 0.700 CausalMutation CLINVAR Frontal lobe epilepsy and mutations of the corticotropin-releasing hormone gene. 16222669

2005
dbSNP: rs72556399
rs72556399
CRH
G 0.700 CausalMutation CLINVAR Frontal lobe epilepsy and mutations of the corticotropin-releasing hormone gene. 16222669

2005
dbSNP: rs121909580
rs121909580
CHRNA4
A 0.700 CausalMutation CLINVAR

dbSNP: rs1554514507
rs1554514507
CHRNA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs281865066
rs281865066
CHRNA4
A 0.700 CausalMutation CLINVAR

dbSNP: rs281865069
rs281865069
CHRNB2
G 0.700 CausalMutation CLINVAR

dbSNP: rs281865070
rs281865070
CHRNB2
C 0.700 CausalMutation CLINVAR

dbSNP: rs281865071
rs281865071
CHRNB2
G 0.700 CausalMutation CLINVAR

dbSNP: rs74315291
rs74315291
CHRNB2
T 0.700 CausalMutation CLINVAR

dbSNP: rs74315291
rs74315291
CHRNB2
C 0.700 CausalMutation CLINVAR