Disease: Epilepsy, Rolandic ×
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: rs180922748
rs180922748 		1.000 0.040 2 166233432 missense variant G/C snv 1.2E-03 1.7E-03
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		Nervous System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs199692186
rs199692186 		1.000 0.040 2 166272748 missense variant T/C snv 6.3E-04 5.5E-04
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		Nervous System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs765818027
rs765818027 		1.000 0.040 2 166293358 missense variant C/T snv 4.6E-05 2.8E-05
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		Nervous System Diseases 0.010 1.000 1 2019 2019