rs10157763, AKT3

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 1.000 0.040 1 243831739 intron variant T/A;C snv 0.010 1.000 1 2016 2016
Epileptic Seizures
CUI: C4317109
Disease: Epileptic Seizures
7 1.000 0.040 1 243831739 intron variant T/A;C snv 0.010 1.000 1 2016 2016