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: rs672601376
rs672601376
0.925 0.040 12 13608760 missense variant A/C snv
CUI: C0014547
Disease: Epilepsies, Partial
Epilepsies, Partial
Nervous System Diseases 0.010 1.000 1 2014 2014
dbSNP: rs672601378
rs672601378
0.882 0.040 12 13615149 missense variant C/T snv
CUI: C0014547
Disease: Epilepsies, Partial
Epilepsies, Partial
Nervous System Diseases 0.010 1.000 1 2014 2014