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: rs41307846
rs41307846
1.000 0.040 1 2028260 missense variant G/A snv 1.7E-02 1.7E-02
CUI: C0270850
Disease: Idiopathic generalized epilepsy
Idiopathic generalized epilepsy
Nervous System Diseases 0.010 1.000 1 2005 2005