Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555955296
rs1555955296
CDKL5
T 0.700 CausalMutation CLINVAR

dbSNP: rs28935468
rs28935468
MECP2
A 0.700 CausalMutation CLINVAR

dbSNP: rs753635972
rs753635972
MTHFS ; ST20-MTHFS
T 0.700 GeneticVariation CLINVAR

dbSNP: rs771379232
rs771379232
MTHFS ; ST20-MTHFS
A 0.700 GeneticVariation CLINVAR

dbSNP: rs886039469
rs886039469
KCNMA1 ; KCNMA1-AS1
C 0.700 CausalMutation CLINVAR

dbSNP: rs763616736
rs763616736
CACNA1G
0.010 GeneticVariation BEFREE One variant, c.1709C>T (Ala570Val), is present in a sporadic case of juvenile myoclonic epilepsy (JME) with early childhood absence and astatic seizures, but was not found in control samples. 17397049

2007