rs3773364, SYN2

N. diseases: 2
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.
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.925 0.040 3 12148468 intron variant A/G snv 0.15 0.030 0.667 3 2010 2015
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