Disease: Epilepsies, Partial ×
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: rs12987787
rs12987787 		1.000 0.040 2 166001881 intron variant T/C snv
CUI: C0014547
Disease: Epilepsies, Partial
Epilepsies, Partial 		Nervous System Diseases 0.700 1.000 1 2014 2014
dbSNP: rs2212656
rs2212656 		1.000 0.040 2 166144333 intron variant C/A;T snv
CUI: C0014547
Disease: Epilepsies, Partial
Epilepsies, Partial 		Nervous System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs121917993
rs121917993 		0.851 0.040 2 165994212 missense variant G/A snv
CUI: C0014547
Disease: Epilepsies, Partial
Epilepsies, Partial 		Nervous System Diseases 0.010 1.000 1 2015 2015
dbSNP: rs3812718
rs3812718 		0.776 0.240 2 166053034 splice region variant C/T snv 0.48
CUI: C0014547
Disease: Epilepsies, Partial
Epilepsies, Partial 		Nervous System Diseases 0.010 1.000 1 2012 2012