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 2 166036278 missense variant C/T snv 0.73 0.74 0.020 1.000 2 2009 2017
idiopathic epilepsy
CUI: C0391957
Disease: idiopathic epilepsy
3 0.925 0.040 2 166036278 missense variant C/T snv 0.73 0.74 0.010 1.000 1 2014 2014
Seizures
CUI: C0036572
Disease: Seizures
553 0.925 0.040 2 166036278 missense variant C/T snv 0.73 0.74 0.010 1.000 1 2012 2012