Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1057519525
rs1057519525
1.000 0.040 2 165308760 missense variant T/G snv
CUI: C0014547
Disease: Epilepsies, Partial
Epilepsies, Partial
Nervous System Diseases 0.700 0
dbSNP: rs17183814
rs17183814
0.827 0.120 2 165295879 splice acceptor variant G/A snv 8.4E-02 6.2E-02
CUI: C0014547
Disease: Epilepsies, Partial
Epilepsies, Partial
Nervous System Diseases 0.010 1.000 1 2019 2019