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: rs143166100
rs143166100
1.000 0.040 9 128607988 missense variant C/G snv 5.7E-04 5.4E-04
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic
Nervous System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1441152520
rs1441152520
1.000 0.040 9 128632218 missense variant A/G snv
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic
Nervous System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1554759745
rs1554759745
1.000 0.040 9 128611792 missense variant G/A snv
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic
Nervous System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs569997507
rs569997507
1.000 0.040 9 128604371 missense variant C/T snv 4.0E-05 4.2E-05
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic
Nervous System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs780658554
rs780658554
1.000 0.040 9 128584312 missense variant C/T snv 3.2E-05 3.5E-05
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic
Nervous System Diseases 0.700 1.000 1 2018 2018