Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs796053228
rs796053228
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
T 0.720 CausalMutation CLINVAR

dbSNP: rs959316981
rs959316981
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
T 0.700 GeneticVariation CLINVAR

dbSNP: rs886041874
rs886041874
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
C 0.700 GeneticVariation CLINVAR

dbSNP: rs886041715
rs886041715
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
C 0.700 GeneticVariation CLINVAR

dbSNP: rs879255709
rs879255709
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
A 0.700 CausalMutation CLINVAR

dbSNP: rs879253767
rs879253767
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
C 0.700 CausalMutation CLINVAR

dbSNP: rs879253748
rs879253748
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
T 0.700 CausalMutation CLINVAR

dbSNP: rs878853250
rs878853250
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
C 0.700 CausalMutation CLINVAR

dbSNP: rs869312702
rs869312702
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
A 0.700 GeneticVariation CLINVAR

dbSNP: rs796053367
rs796053367
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
T 0.700 CausalMutation CLINVAR

dbSNP: rs796053366
rs796053366
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
T 0.700 CausalMutation CLINVAR

dbSNP: rs796053335
rs796053335
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
GGCATGC 0.700 CausalMutation CLINVAR

dbSNP: rs796053216
rs796053216
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
A 0.700 GeneticVariation CLINVAR

dbSNP: rs796053130
rs796053130
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
T 0.700 GeneticVariation CLINVAR

dbSNP: rs796053083
rs796053083
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
C 0.700 CausalMutation CLINVAR

dbSNP: rs796052957
rs796052957
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
G 0.700 GeneticVariation CLINVAR

dbSNP: rs794727444
rs794727444
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
A 0.700 CausalMutation CLINVAR

dbSNP: rs794726754
rs794726754
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
T 0.700 CausalMutation CLINVAR

dbSNP: rs786204967
rs786204967
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
C 0.700 CausalMutation CLINVAR

dbSNP: rs775162839
rs775162839
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
T 0.700 CausalMutation CLINVAR

dbSNP: rs764618040
rs764618040
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
T 0.700 GeneticVariation CLINVAR

dbSNP: rs763777257
rs763777257
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
A 0.700 CausalMutation CLINVAR

dbSNP: rs759766243
rs759766243
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
A 0.700 GeneticVariation CLINVAR

dbSNP: rs747824231
rs747824231
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
G 0.700 CausalMutation CLINVAR

dbSNP: rs587777848
rs587777848
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
C 0.700 CausalMutation CLINVAR