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: rs211037
rs211037
0.742 0.240 5 162101274 synonymous variant C/T snv 0.28 0.31
CUI: C0270850
Disease: Idiopathic generalized epilepsy
Idiopathic generalized epilepsy
Nervous System Diseases 0.020 1.000 2 2013 2018