Disease: Epilepsy ×
Source: ALL
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: rs4906902
rs4906902 		0.724 0.200 15 26774621 intron variant A/G snv 0.15
CUI: C0014544
Disease: Epilepsy
Epilepsy 		Nervous System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs572427454
rs572427454 		0.882 0.080 15 26560943 missense variant C/T snv 2.8E-05 1.4E-05
CUI: C0014544
Disease: Epilepsy
Epilepsy 		Nervous System Diseases 0.010 1.000 1 2019 2019