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: rs11890028
rs11890028 		1.000 0.040 2 166086767 intron variant T/A;G snv
CUI: C0014548
Disease: Epilepsy, Generalized
Epilepsy, Generalized 		Nervous System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs121917953
rs121917953 		0.851 0.080 2 166054677 missense variant T/A snv
CUI: C0014548
Disease: Epilepsy, Generalized
Epilepsy, Generalized 		Nervous System Diseases 0.010 1.000 1 2003 2003
dbSNP: rs121917986
rs121917986 		0.882 0.040 2 166002588 missense variant C/G;T snv
CUI: C0014548
Disease: Epilepsy, Generalized
Epilepsy, Generalized 		Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs121918628
rs121918628 		0.851 0.080 2 165998049 missense variant G/T snv
CUI: C0014548
Disease: Epilepsy, Generalized
Epilepsy, Generalized 		Nervous System Diseases 0.010 1.000 1 2008 2008