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: rs1130183
rs1130183
0.827 0.160 1 160041722 missense variant G/A snv 4.6E-02 4.7E-02
CUI: C0270850
Disease: Idiopathic generalized epilepsy
Idiopathic generalized epilepsy
Nervous System Diseases 0.010 1.000 1 2005 2005
dbSNP: rs2486253
rs2486253
0.882 0.080 1 160039629 3 prime UTR variant A/C;T snv
CUI: C0270850
Disease: Idiopathic generalized epilepsy
Idiopathic generalized epilepsy
Nervous System Diseases 0.010 1.000 1 2015 2015