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: rs80356616
rs80356616
0.732 0.360 11 17387917 missense variant C/T snv
CUI: C0014548
Disease: Epilepsy, Generalized
Epilepsy, Generalized
Nervous System Diseases 0.010 1.000 1 2006 2006