rs2279020, GABRA1

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 5 161895883 non coding transcript exon variant G/A snv 0.62 0.63 0.030 1.000 3 2010 2016
Seizures
CUI: C0036572
Disease: Seizures
553 1.000 0.040 5 161895883 non coding transcript exon variant G/A snv 0.62 0.63 0.010 1.000 1 2010 2010