Disease: Epilepsy, Generalized ×
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: rs11943905
rs11943905 		1.000 0.040 4 46395600 intron variant C/T snv 0.22
CUI: C0014548
Disease: Epilepsy, Generalized
Epilepsy, Generalized 		Nervous System Diseases 0.700 1.000 1 2018 2018