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: rs4906902
rs4906902
0.724 0.200 15 26774621 intron variant A/G snv 0.15
CUI: C0014548
Disease: Epilepsy, Generalized
Epilepsy, Generalized
Nervous System Diseases 0.010 1.000 1 2011 2011