rs3773364, SYN2

N. diseases: 2
Disease: idiopathic epilepsy ×
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
idiopathic epilepsy
CUI: C0391957
Disease: idiopathic epilepsy
3 0.925 0.040 3 12148468 intron variant A/G snv 0.15 0.010 1.000 1 2010 2010